陳持平醫師論文清單

Jan-Gowth Chang, Long-Shyong Lee, Che-Pin Lin, Pao-Huei Chen, Chih-Ping Chen. Rapid diagnosis of alpha-thalassemia-1 of Southeast Asia type and hydrops fetalis by polymerase chain reaction. Blood 1991; 78: 853-854.

Jan-Gowth Chang, Long-Shyong Lee, Che-Pin Lin, Pao-Huei Chen, Chih-Ping Chen. Rapid diagnosis of alpha-thalassemia-1 of Southeast Asia type and hydrops fetalis by polymerase chain reaction. Blood 1991; 78: 853-854.

Jan-Gowth Chang, Chih-Ping Chen, Huey-Jane Ho, Che-Pin Lin, Long-Shyong Lee, Pao-Huei Chen. Rapid prenatal diagnosis of Hb Bart’s hydrops fetalis in southeast Asia area by polymerase chain reaction. Int J Hematol 1992; 56: 155-159.

Jui-Der Liou, Chih-Ping Chen, W. Roy Breg, John C. Hobbins, Maurice J. Mahoney, Teresa L. Yang-Feng. Fetal blood sampling and cytogenetic abnormalities. Prenat Diagn 1993; 13: 1-8.

Fon-Jou Hsieh, Ming-Kwang Shyu, Bor-Ching Sheu, Shen-Pei Lin, Chih-Ping Chen, Fu-Yuan Huang. Limb defects after chorionic villus sampling. Obstet Gynecol 1995; 85: 84-88.

Chih-Ping Chen, Sheau-Wen Jan, Fen-Fen Liu, Sheng Chiang, Shih-Hung Huang, Jin-Cherng Sheu, Kuo-Gon Wang, Chung-Chi Lan. Prenatal diagnosis of omphalocele associated with umbilical cord cyst. Acta Obstet Gynecol Scand 1995; 74: 832-835.

Chih-Ping Chen, Sheau-Wen Jan, Fen-Fen Liu, Jin-Cherng Sheu, Shih-Hung Huang. Echo-guided lymphatic drainage by fine-needle aspiration in persistent isolated septated fetal nuchal cystic hygroma. Fetal Diagn Ther 1996; 11: 150-153.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Shuan-Pei Lin, Chung-Chi Lan. Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of the long bones and a single umbilical artery. Prenat Diagn 1996; 16: 270-275.

Sheau-Wen Jan, Chih-Ping Chen, Lian-Hua Huang, Fu-Yuan Huang, Chung-Chi Lan. Attitudes toward maternal serum screening in Chinese women with positive results. J Genet Counsel 1996; 5: 169-180.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Chao-Wen Chen, Kuo-Gon Wang, Chung-Chi Lan. Prenatal detection of the separation of the great toe, toe syndactyly, and large bilateral choroid plexus cysts in a fetus with trisomy 18. Am J Perinatol 1996; 13: 203-205.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Chen-Chi Lee, Dai-Dyi Town, Chung-Chi Lan. Cytogenetic evaluation of cystic hygroma associated with hydrops fetalis, oligohydramnios or intrauterine fetal death: the roles of amniocentesis, postmortem chorionic villus sampling and cystic hygroma paracentesis. Acta Obstet Gynecol Scand 1996; 75: 454-458.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Shuan-Pei Lin, Chung-Chi Lan. CVS-exposed limb deficiency defects with or without other birth defects: presentation of six cases born during a period of nine years. Am J Med Genet 1996; 63: 447-453.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Pei-Yeh Chang, Yun-Nan Lin, Chung-Chi Lan. Ultrasound-guided fluid aspiration and prenatal diagnosis of duplicated hydrometrocolpos with uterus didelphys and septate vagina. Prenat Diagn 1996; 16: 572-576.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Chie-Pein Chen, Chung-Chi Lan. Partial duplication of 3q and distal deletion of 11q in a stillbirth with an omphalocele containing the liver, short limbs, and intrauterine growth retardation. J Med Genet 1996; 33: 615-617.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Kuo-Gon Wang, Chung-Chi Lan. Prenatal diagnosis of partial monosomy 13q associated with occipital encephalocoele in a fetus. Prenat Diagn 1996; 16: 664-666.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Jin-Cherng Sheu, Shih-Hung Huang, Chung-Chi Lan. Prenatal diagnosis and perinatal aspects of abdominal wall defects. Am J Perinatol 1996; 13: 355-361.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Tsung-Hsien Su, Chung-Chi Lan. A concealed penis mimicking penile agenesis in an infant with trisomy 13. Clin Genet 1996; 50: 156-158.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Yun-Nan Lin, Chung-Chi Lan. A case of achondrogenesis type IA with an occipital encephalocele. Genet Couns 1996; 7: 193-199.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Chen-Li Lin, Chung-Chi Lan. Prenatal diagnosis of terminal deletion 7q and partial trisomy 3p in fetuses with holoprosencephaly. Clin Genet 1996; 50: 321-326.

Chih-Ping Chen, Shuan-Pei Lin, Fen-Fen Liu, Sheau-Wen Jan, Shyr-Yeu Lin, Chung-Chi Lan. Prenatal diagnosis of asphyxiating thoracic dysplasia (Jeune syndrome). Am J Perinatol 1996; 13: 495-498.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Yuh-Cheng Yang, Chung-Chi Lan. Prenatal diagnosis of supernumerary der(22)t(11;22) associated with the Dandy-Walker malformation in a fetus. Prenat Diagn 1996; 16: 1137-1140.

Chih-Ping Chen, Shin-Lin Shih, Fen-Fen Liu, Sheau-Wen Jan, Tsuen-Chiuan Tsai, Pei-Yeh Chang, Chung-Chi Lan. In utero urinary bladder perforation, urinary ascites and bilateral contained urinomas secondary to posterior urethral valves: clinical and imaging findings. Pediatr Radiol 1997; 27: 3-5.

Chih-Ping Chen, Fen-Fen Liu, Sheau-Wen Jan, Kuo-Gon Wang, Chung-Chi Lan. First report of distal obstructive uropathy and prune-belly syndrome in an infant with amniotic band syndrome. Am J Perinatol 1997; 14: 31-33

Chih-Ping Chen, Hsiu-Chin Chen,Fen-Fen Liu, Sheau-Wen Jan, Shuan-Pei Lin, Jin-Cherng Sheu, Be-Fong Chen. Progressive fetal axillary cystic lymphangioma with coexistent naevus flammeus. Br J Dermatol 1997; 136: 102-104.

Chih-Ping Chen, Schu-Rern Chern, Fen-Fen Liu, Sheau-Wen Jan, Hung-Chang Lee, Jin-Cherng Sheu, Wen-Ta Lee, Tao-Yeuan Wang. Prenatal diagnosis, pathology, and genetic study of fetus in fetu. Prenat Diagn 1997; 17: 13-21.

Chih-Ping Chen, Hsiu-Chin Chen, Fen-Fen Liu, Sheau-Wen Jan, Schu-Rern Chern, Tao-Yeuan Wang, Han-Yang Hung. Cutis marmorata telangiectatica congenita associated with an elevated maternal serum human chorionic gonadotrophin level and transitory isolated fetal ascites. Br J Dermatol 1997; 136: 267-271.

Chih-Ping Chen, Shin-Lin Shih, Fen-Fen Liu, Sheau-Wen Jan, Yun-Nan Lin, Chung-Chi Lan. Skeletal deformities of acardius anceps: the gross and imaging features. Pediatr Radiol 1997; 27: 221-225.

Chih-Ping Chen, Shin-Lin Shih, Fen-Fen Liu, Sheau-Wen Jan. Cebocephaly, alobar holoprosencephaly, spina bifida and sirenomelia in a stillbirth. J Med Genet 1997; 34: 252-255.

Chih-Ping Chen, Chin-Cheng Lee, Fen-Fen Liu, Sheau-Wen Jan, Ming-Huei Lin, Be-Fong Chen. Prenatal diagnosis of cephalothoracopagus janiceps monosymmetros. Prenat Diagn 1997; 17: 384-388

Chih-Ping Chen, Chun-Yu Chuang, Yi-Chin Chang, Chi-Yuan Tzen. Type III congenital cystic adenomatoid malformation of the lung detected through maternal serum screening positive for Down’s syndrome. Acta Obstet Gynecol Scand 1997; 76: 378-379.

Chih-Ping Chen, Shin-Lin Shih, Fen-Fen Liu, Sheau-Wen Jan, Cherng-Jye Jeng, Chung-Chi Lan. Perinatal features of Omphalocele-Exstrophy-Imperforate anus-Spinal defects (OEIS complex) associated with large meningomyeloceles and severe limb defects. Am J Perinatol 1997; 14: 275-279.

Chih-Ping Chen, Schu-Rern Chern, Fen-Fen Liu, Sheau-Wen Jan, Chen-Chi Lee, Yi-Chin Chang, Chung-Tai Yue. Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive results. Prenal Diagn 1997; 17: 571-576.

Chih-Ping Chen, Cheng-Chun Lin, Chun-Yu Chuang, Chen-Chi Lee, Wen-Lin Chen, Sheau-Wen Jan, Shuan-Pei Lin. Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21)(p13.3;q21). Prenat Diagn 1997; 17: 675-680.

Chih-Ping Chen, Shu-Huey Chen, Chun-Yu Chuang, Hung-Chang Lee, Yuh-Ming Hwu, Pei-Yeh Chang, Mong-Liang Chen, Be-Fong Chen. Clinical and perinatal sonographic features of congenital adrenal cystic neuroblastoma: a case report with review of the literature. Ultrasound Obstet Gynecol 1997; 10: 68-73.

Chih-Ping Chen, Chen-Chi Lee, Li-Feng Chen, Chun-Yu Chuang, Sheau-Wen Jan, Be-Fong Chen. Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephaly. J Med Genet 1997;34:777-778.

Chih-Ping Chen, Chen-Chi Lee, Chun-Yu Chuang, Dai-Dyi Town, Meng-Shan Lee, Ming-Hong Chen. Recurrent omphalocele with partial trisomy 3q and partial monosomy 11q. Clin Genet 1997; 52: 196-198.

Chih-Ping Chen, Schu-Rern Chern, Tao-Yeuan Wang, Zon-Darr Huang, Ming-Chao Huang, Chun-Yu Chuang. Pregnancy with concomitant chorangioma and placental vascular malformation with mesenchymal hyperplasia. Hum Reprod 1997; 12: 2553-2556.

Chih-Ping Chen, Shuan-Pei Lin. Maternal serum screening abnormality in a fetus associated with arthrogryposis multiplex congenita and amyoplasia. Prenat Diagn 1997; 17: 1187-1188.

Chih-Ping Chen, Schu-Rern Chern, Shin-Lin Shih, Chun-Yu Chuang, Fu-Yuan Huang. Kyphomelic dysplasia in two sib fetuses. J Med Genet 1998; 35: 65-69.

Chih-Ping Chen, Tai-Ho Hung, Sheau-Wen Jan, Cherng-Jye Jeng. Enlarged cisterna magna in the third trimester as a clue to fetal trisomy 18. Fetal Diagn Ther 1998; 13:29-34.

Chih-Ping Chen, Shin-Lin Shih, Chun-Yu Chuang, Jin-Cherng Sheu, Be-Fong Chen. In utero adrenal hemorrhage: clinical and imaging findings. Acta Obstet Gynecol Scand 1998; 77: 239-241.

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Li-Feng Chen, Chun-Yu Chuang, Ming-Hong Chen. Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus. Prenat Diagn 1998;18: 393-398.

Chih-Ping Chen, Tao-Yeuan Wang, Chun-Yu Chuang. Sonographic findings in a fetus with megacystis-microcolon-intestinal hypoperistalsis syndrome. J Clin Ultrasound 1998; 26: 217-220.

Chih-Ping Chen, Schu-Rern Chern, Chun-Yu Chuang, Be-Fong Chen. Prenatal detection of human cytomegalovirus DNA in fetal ascites by the polymerase chain reaction. Acta Obstet Gynecol Scand 1998; 77: 466-467.

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Li-Feng Chen, Chun-Yu Chuang. Prenatal diagnosis of de novo interstitial 16q deletion in a fetus associated with sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the long bones. Prenat Diagn 1998; 18: 490-495.

Koen Devriendt, Jean-Pierre Fryns, Chih-Ping Chen. Holoprosencephaly in deletions of proximal chromosome 14q. J Med Genet 1998, 35:612.

Chih-Ping Chen, Shin-Lin Shih, Sheau-Wen Jan, Yun-Nan Lin. Sirenomelia with an uncommon osseous fusion associated with a neural tube defect. Pediatr Radiol 1998; 28: 293-296.

Chih-Ping Chen, Schu-Rern Chern, Shuan-Pei Lin, Pei-Yeh Chang, Kuo-Ming Chang, Fon-Jou Hsieh. Concomitant chyloperitoneum and omental cysts presenting as fetal ascites with intra-abdominal cysts on prenatal ultrasound. Prenat Diagn 1998; 18: 984-986.

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Dai-Dyi Town. Isochromosome 18q in a fetus with congenital megacystis, intra-uterine growth retardation and cloacal dysgenesis sequence. Prenat Diagn 1998; 18: 1068-1074.

Chih-Ping Chen, Wayseen Wang, Shuan-Pei Lin, Jin-Cherng Sheu, Chi-Yuan Tzen. Favorable outcome in a fetus with an early-onset extensive cystic hygroma colli and intralesional hemorrhage. Am J Perinatol 1998; 15: 601-605.

Chih-Ping Chen, Tsu-Chi Hsu, Wayseen Wang. Ileal penetration by a Multiload-Cu 375 intrauterine contraceptive device: a case report with review of the literature. Contraception 1998; 58: 295-304.

Chih-Ping Chen, Wayseen Wang, Shuan-Pei Lin, Jin-Cherng Sheu, Jeng-Daw Tsai. Perinatal findings in a male fetus with congenital megacystis and anorectal malformations. Fetal Diagn Ther 1998; 13: 348-351.

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Wen-Lin Chen, Ming-Hong Chen, Kuo-Ming Chang. De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy and partial hemihypoplasia. J Med Genet 1998; 35: 1050-1053.

Chih-Ping Chen, Chen-Chi Lee, Chen-Wen Pan, Twan-Yin Kir, Be-Fong Chen. Partial trisomy 8q and partial monosomy 15q associated with hydrocephalus, congenital diaphragmatic hernia, urinary tract anomalies, congenital heart defect and kyphoscoliosis. Prenat Diagn 1998; 18: 1289-1293.

Yuh-Ming Hwu, Robert Kuo-kuang Lee, Chih-Ping Chen, Jing-Tsung Su, Yu-Wen Chen, Shau-Ping Lin. Development of hatching blastocysts from immature human oocytes following in-vitro maturation and fertilization using a co-culture system. Hum Reprod 1998; 13: 1916-1921.

Chih-Ping Chen, Schu-Rern Chern, Tao-Yeung Wang, Wayseen Wang, Kung-Liahng Wang, Cherng-Jye Jeng. Androgen receptor gene mutations in 46,XY females with germ cell tumors. Hum Reprod 1999; 14: 664-670.

Chih-Ping Chen. Inconsistency of omphalocele contents in three consecutive siblings with partial trisomy 3q and partial monosomy 11q. Prenat Diagn 1999; 19: 591.

Chih-Ping Chen, Schu-Rern Chern, Tao-Yeuan Wang, Wayseen Wang, Yuh-Ming Hwu. A frame shift mutation in the DNA-binding domain of the androgen receptor gene associated with complete androgen insensitivity, persistent müllerian structures, and germ cell tumors in dysgenetic gonads. Fertil Steril 1999; 72:170-173.

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Wayseen Wang. Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3;p13.2). Prenat Diagn 1999; 19: 783-786.

Chih-Ping Chen, Jin-Chung Shih, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang, Tao-Yeuan Wang. Prenatal diagnosis of a fetus with distal 10q trisomy. Prenat Diagn 1999; 19: 876-878.

Chih-Ping Chen. Congenital cervical cystic hygroma causing an airway emergency. Am J Emerg Med 1999; 17: 622-624.

Chih-Ping Chen, Koenraad Devriendt, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang, Tao-Yeuan Wang. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia. Prenat Diagn 1999; 19: 986-989.

Chih-Ping Chen, Wayseen Wang, Tao-Yeuan Wang. Adnexal torsion during late pregnancy. Am J Emerg Med 1999; 17: 738-739.

Chih-Ping Chen, Jin-Chung Shih. Prenatal diagnosis of bilateral ventriculomegaly and an enlarged cisterna magna in a fetus with partial trisomy 9 and partial trisomy 21. Prenat Diagn 1999; 19: 1175-1180.

Chih-Ping Chen, Chin-Yuan Tzen, Wayseen Wang. Prenatal diagnosis of cystic bladder distension secondary to obstructive uropathy. Prenat Diagn 2000; 20: 260-263.

Chih-Ping Chen, Chin-Yuan Tzen, Shin-Lin Shih, Li-Fan Yeh, Wayseen Wang. A fetus with VACTERL association, unilateral aplasia of the humerus and partial hemihypoplasia. Clin Dysmorphol 2000; 9: 147-148.

Chih-Ping Chen, Schu-Rern Chern, Wayseen Wang. Rapid determination of zygosity and common aneuploidies from amniotic fluid cells using quantitative fluorescent polymerase chain reaction following genetic amniocentesis in multiple pregnancies. Hum Reprod 2000; 15: 929-934.

Chih-Ping Chen, Schu-Rern Chern, Wayseen Wang. Fetal DNA in maternal plasma: the prenatal detection of a paternally inherited fetal aneuploidy. Prenat Diagn 2000; 20: 355-357.

Chih-Ping Chen, Min-Hui Wang, Li-Fan Yeh, Wayseen Wang. Rapid diagnosis and treatment of post-cesarean parametrial abscess by transabdominal ultrasound-guided needle aspiration. Ultrasound Obstet Gynecol 2000; 15: 343-344.

Chih-Ping Chen, Koenraad Devriendt, Schu-Rern Chern, Chen-Chi Lee, Wayseen Wang, Shuan-Pei Lin. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes. Prenat Diagn 2000; 20: 384-389.

Schu-Rern Chern, Chih-Ping Chen. Molecular prenatal diagnosis of thalassemia in Taiwan. Int J Obstet Gynecol 2000; 69: 103-106.

Chih-Ping Chen, Schu-Rern Chern, Be-Fong Chen, Wayseen Wang, Yuh-Ming Hwu. Hamartoma in a pubertal patient with complete androgen insensitivity syndrome and R(831)X mutation of the androgen receptor gene. Fertil Steril 2000; 74: 182-183.

Chih-Ping Chen, Schu-Rern Chern, Li-Fan Yeh, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18. Prenat Diagn 2000; 20: 750-753.

Chih-Ping Chen, Schu-Rern Chern, Chih-Long Chang, Chen-Chi Lee, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and genetic analysis of X chromosome polysomy 49,XXXXY. Prenat Diagn 2000; 20: 754-757.

Chih-Ping Chen. A digynic triploid fetus presenting with intrauterine growth restriction, severe oligohydramnios and relative macrocephaly on prenatal ultrasound. Ultrasound Obstet Gynecol 2000; 16: 291-292.

Chih-Ping Chen. Cytogenetic discrepancy between fetal tissue and body fluid in a fetus with cystic hygroma colli. Prenat Diagn 2000; 20: 933-934.

Chih-Ping Chen, Jin-Chung Shih, Yu-Jan Chan. Prenatal diagnosis of limb-body wall complex using two- and three-dimensional ultrasound. Prenat Diagn 2000; 20: 1020.

Chih-Ping Chen. Severe terminal transverse limb reduction defects in homozygous Southeast-Asian alpha-thalassaemia-1. Clin Dysmorphol 2001; 9: 71-73.

Chih-Ping Chen. Prenatal diagnosis of partial trisomy 3q(3q22-->qter) and monosomy 6q(6q25.3-->qter) in a fetus with sonographic findings of cystic hygromata colli and unilateral pleural effusion. Prenat Diagn 2001; 21: 73.

Chih-Ping Chen, Schu-Rern Chern, Jin-Chung Shih, Wayseen Wang, Li-Fan Yeh, Tung-Yao Chang, Chin-Yuan Tzen. Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia. Prenat Diagn 2001; 21: 89-95.

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly. Prenat Diagn 2001; 21: 102-105.

Jin-Chung Shih, Chih-Ping Chen, Fon-Jou Hsieh. Three-dimensional ultrasonography in genetic screening and counselling. Ultrasound Rev Obstet Gynecol 2001; 2: 120-127.

Chih-Ping Chen. Ultrasound-guided needle aspiration of a fetal choledochal cyst. Ultrasound Obstet Gynecol 2001; 17: 175-176.

Chih-Ping Chen, Schu-Rern Chern, Wayseen Wang, Kung-Liahng Wang, Tao-Yeuan Wang. Multiple globules in a cystic ovarian teratoma. Fertil Steril 2001; 75: 618-619.

Chih-Ping Chen, Schu-Rern Chern, Wayseen Wang, Tao-Yeuan Wang. Second-trimester molecular diagnosis of a heterozygous 742C→T (R248C) mutation in the FGFR3 gene in a thanatophoric dysplasia variant following suspicious ultrasound findings. Ultrasound Obstet Gynecol 2001; 17: 272-273.

Chih-Ping Chen. First-trimester sonographic demonstration of a mobile cranial cyst associated with anencephaly and amniotic band sequence. Ultrasound Obstet Gynecol 2001; 17: 360-361.

Chih-Ping Chen, Schu-Rern Chern, Chin-Yuan Tzen, Meng-Shan Lee, Chen-Wen Pan, Tung-Yao Chang, Wayseen Wang. Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts. Prenat Diagn 2001; 21: 317-320.

Chih-Ping Chen, Schu-Rern Chern, Wayseen Wang, Chen-Chi Lee, Wen-Lin Chen, Li-Feng Chen, Tung-Yao Chang, Chin-Yuan Tzen. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis. Prenat Diagn 2001; 21: 346-350.

Chih-Ping Chen. Prenatal diagnosis of limb-body wall complex with craniofacial defects, amniotic bands, adhesions and upper limb deficiency. Prenat Diagn 2001; 21: 418-419.

Chih-Ping Chen, Schu-Rern Chern, Wayseen Wang. Fetal DNA analyzed in plasma from a mother’s three consecutive pregnancies to detect paternally inherited aneuploidy. Clin Chem 2001; 47: 937-939.

Chih-Ping Chen, Hung-Kung Chang, Chin-Yin Sheu, Be-Fong Chen, Shing-Jyh Chang, Wayseen Wang. Sonographic detection of previously unsuspected vesical endometriosis in a woman with dysmenorrhea. Ultrasound Obstet Gynecol 2001; 18: 183-184.

Chih-Ping Chen, Tung-Yao Chang, Wayseen Wang. Resolution of fetal bilateral chylothorax and ascites after two unilateral thoracocenteses. Ultrasound Obstet Gynecol 2001; 18: 401-402.

Chih-Ping Chen. Use of the hemostatic multiple square suturing of the uterus for control of massive postcesarean section hemorrhage and preservation of fertility. Acta Obstet Gynecol Scand 2001; 80: 976.

Chih-Ping Chen, Chi-Yuan Tzen. Short-rib polydactyly syndrome type III (Verma-Naumoff) in a third-trimester fetus with unusual associations of epiglottic hypoplasia, renal cystic dysplasia, pyelectasia and oligohydramnios. Prenat Diagn 2001; 21: 1101-1102.

Chih-Ping Chen, Schu-Rern Chern, Shin-Hua Du, Wayseen Wang. Molecular diagnosis of a novel heterozygous 268C-->T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis. Prenat Diagn 2002; 22: 5-7.

Chih-Ping Chen, Jin-Chung Shih, Chin-Yuan Tzen, Wayseen Wang. Three-dimensional ultrasound in the evaluation of complex anomalies associated with fetal ventral midline defects. Ultrasound Obstet Gynecol 2002; 19: 102-104.

Chih-Ping Chen, Jin-Cherng Sheu, Wayseen Wang, Shuan-Pei Lin, Tung-Yao Chang, Chin-Yuan Tzen. Fetal cervico-mediastinal cystic hygroma associated with maternal serum screening positive for Down syndrome. Prenat Diagn 2002; 22: 166.

Chih-Ping Chen, Tung-Yao Chang, Li-Fan Yeh, Chen-Ju Lin, Wayseen Wang. Sonographic appearance of the uterus after simple square suturing for rapid control of postpartum hemorrhage and preservation of fertility. J Clin Ultrasound 2002; 30: 189-191.

Chih-Ping Chen. Prenatal sonographic diagnosis of median facial cleft should alert holoprosencephaly with premaxillary agenesis and prompt genetic investigations. Ultrasound Obstet Gynecol 2002; 19: 421-422.

Chih-Ping Chen, Jin-Cherng Sheu, Shuan-Pei Lin, Chen-Ju Lin, Yu-Jan Chan, Wayseen Wang. Sonographic findings in a case of congenital pyloric diaphragm. Ultrasound Obstet Gynecol 2002; 19: 528-529.

Chih-Ping Chen, Yuh-Cherng Yang, Shuan-Pei Lin, Wayseen Wang, Chih-Long Chang, Kuo-Ming Chang. Bilateral calcified ovarian fibromas in a patient with Sotos syndrome. Fertil Steril 2002; 77: 1285-1287.

Chih-Ping Chen, Tung-Yao Chang, Chi-Yuan Tzen, Chen-Ju Lin, Wayseen Wang. Sonographic detection of situs inversus, ventricular septal defect, and short-rib polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus not known to be at risk. Ultrasound Obstet Gynecol 2002; 19: 629-631.

Chih-Ping Chen, Chin-Yuan Tzen, Tung-Yao Chang, Li-Fan Yeh, Wayseen Wang. Prenatal diagnosis of acrania associated with facial defects, amniotic bands and limb-body wall complex. Ultrasound Obstet Gynecol 2002; 20: 94-95.

Chih-Ping Chen, Shuan-Pei Lin, Nan-Chang Chiu. Microcephaly with dysgenesis of corpus callosum and colpocephaly in the survivor after the first-trimester death of a monochorionic co-twin. Prenat Diagn 2002; 22:634-636.

Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Chen-Ju Lin, Wayseen Wang, Chin-Yuan Tzen. Second trimester molecular diagnosis of a stop codon FGFR3 mutation in a type I thanatophoric dysplasia fetus following abnormal ultrasound findings. Prenat Diagn 2002; 22: 736-737.

Chih-Ping Chen. Identification of unexpected parental Robertsonian (13q;14q) translocations following prenatal sonographic detection of holoprosencephaly. Ultraosund Obstet Gynecol 2002; 20: 304-305.

Chih-Ping Chen, Hong-Chih Hsu, Schu-Rern Chern, Chin-Yuan Tzen, Wayseen Wang, Chen-Ju Lin. Second-trimester diagnosis of digynic triploidy in a case of anhydramnios and fetal cyclopia by ultrasound-guided transabdominal chorionic villus sampling. Ultrasound Obstet Gynecol 2002; 20: 415-416.

Chih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, Nan-Chang Chiu, Shin-Lin Shih, Chen-Ju Lin, Wayseen Wang, Hong-Chih Hsu. Perinatal imaging findings of inherited Sotos syndrome. Prenat Diagn 2002; 22: 887-892.

Chih-Ping Chen, Tung-Yao Chang, Jin-Chung Shih, Shuan-Pei Lin, Chen-Ju Lin, Wayseen Wang, Chen-Chi Lee, Dai-Dyi Town, Chen-Wen Pan, Chin-Yuan Tzen. Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion. Prenat Diagn 2002, 22: 1063-1066.

Chih-Ping Chen, Chin-Yuan Tzen , Tung-Yao Chang, Chen-Ju Lin, Wayseen Wang, Chen-Chi Lee, Dai-Dyi Town, Li-Feng Chen, Meng-Shan Lee. Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy-Walker variant and trigonocephaly. Prenat Diagn 2002; 22: 1112-1113.

Chih-Ping Chen, Jin-Chung Shih. Prenatal visualization of the vasculature of fetal sacrococcygeal teratoma by three-dimensional color power angiography. Ultrasound Obstet Gynecol 2002; 20: 636-637.

Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Chen-Chi Lee, Li-Feng Chen, Chin-Yuan Tzen, Wayseen Wang, Chen-Ju Lin, Brian P.T. Yang, Lawrence S.T. Yang. Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction. Prenat Diagn 2003; 23: 40-43.

Chih-Ping Chen. Detection of mosaic isochromosome 20q in amniotic fluid in a pregnancy with fetal arthrogryposis multiplex congenita and normal karyotype in fetal blood and postnatal samplings of placenta, skin, and liver. Prenat Diagn 2003; 23: 85-87.

Chih-Ping Chen, Schu-Rern Chern, Shuan-Pei Lin, Wayseen Wang, Fuu-Jen Tsai. Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis. Prenat Diagn 2003; 23: 175-176.

Chih-Ping Chen, Chin-Yuan Tzen, Tung-Yao Chang, Chen-Ju Lin, Wayseen Wang, Chen-Chi Lee, Li-Feng Chen, Wen-Lin Chen. Prenatal diagnosis of de novo mosaic distal 18q deletion associated with congenital anomalies. Ultraosund Obstet Gynecol 2003; 21: 202-204.

Chih-Ping Chen, Jin-Chung Shih, Jon-Kway Huang, Daniel T.H. Chin, Chin-Yuan Tzen, Yi-Hui Lin, Wayseen Wang. Two- and three-dimensional ultrasound demonstration of a giant epignathus. Ultrasound Obstet Gynecol 2003; 21: 407-409.

Chih-Ping Chen, Tung-Yao Chang, Schu-Rern Chern, Dai-Dyi Town, Chen-Wen Pan, Meng-Shan Lee, Wayseen Wang. Early second-trimester diagnosis of monozygotic twins discordant for cystic hygroma colli and Turner syndrome. Prenat Diagn 2003; 23: 352-353.

Chih-Ping Chen, Tung-Yao Chang, Chin-Yuan Tzen, Wayseen Wang. Second-trimester sonographic detection of short rib-polydactyly syndrome type II (Majewski) following an abnormal maternal serum biochemical screening result. Prenat Diagn 2003; 23: 353-355.

Chih-Ping Chen, Yuh-Ming Hwu, Li-Fan Yeh, Schu-Rern Chern, Chen-Chi Lee, Wayseen Wang. Successful triplet pregnancy and delivery after oocyte donation in an infertile female with chromosome mosaicism for monosomy X, partial trisomy X, and terminal Xp deletion. Fertil Steril 2003; 79: 1231-1233.

Chih-Ping Chen, Tung-Yao Chang, Chin-Yuan Tzen, Wayseen Wang, Chen-Chi Lee, Li-Feng Chen, Meng-Shan Lee, Shuan-Pei Lin. Second-trimester sonographic demonstration of retrognathia and bilateral pyelectasis in a fetus with a duplication of chromosome 10q24.1-->qter. Ultraosund Obstet Gynecol 2003; 21: 516-518.

Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Chin-Yuan Tzen, Chen-Chi Lee, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis of de novo terminal deletion of chromosome 7q. Prenat Diagn 2003; 23: 375-379.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Shin-Lin Shih, Chen-Chi Lee, Wayseen Wang, You-Wei Liao. Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion. Prenat Diagn 2003; 23: 504-508.

Chih-Ping Chen, Jin-Chung Shih, Jui-Hsing Chang, Yi-Hui Lin, Wayseen Wang. Prenatal diagnosis of right pulmonary agenesis associated with VACTERL sequence. Prenat Diagn 2003; 23: 515-518.

Chih-Ping Chen. Prenatal diagnosis of de novo partial trisomy Xq (Xq22.1-->qter) and terminal Xp deletion following sonographic detection of intrauterine growth restriction. Prenat Diagn 2003; 23: 518-519.

Chih-Ping Chen, Chyong-Hsin Hsu, Shuan-Pei Lin, Che-Sheng Ho, Chen-Chi Lee, Wayseen Wang. Association of partial trisomy 9 (9pter®q22.3) with corpus callosum dysgenesis, bilateral subependymal cysts and ventriculomegaly. Prenat Diagn 2003; 23: 519-520.

Chih-Ping Chen. Prenatal sonographic diagnosis of limb-body wall complex with craniofacial defects. Ultrasound Obstet Gynecol 2003; 22: 101.

Chih-Ping Chen, Jin-Chung Shih, Jon-Kway Huang, Wayseen Wang, Chin-Yuan Tzen. Second-trimester evaluation of fetal sacrococcygeal teratoma using three-dimensional color Doppler ultrasound and magnetic resonance imaging. Prenat Diagn 2003; 23: 602-603.

Chih-Ping Chen, Kuo-Gon Wang, Jon-Kway Huang, Tung-Yao Chang, Yi-Hui Lin, Daniel T.H. Chin, Chin-Yuan Tzen, Wayseen Wang. Prenatal diagnosis of otocephaly with microphthalmia/anophthalmia using ultrasound and magnetic resonance imaging. Ultrasound Obstet Gynecol 2003; 22: 214-215.

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Li-Feng Chen, Daniel T.H. Chin, Chin-Yuan Tzen, Wayseen Wang. Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion. Prenat Diagn 2003; 23: 758-761.

Chih-Ping Chen. Congenital retroperitoneal cystic teratoma mimicking a cystic lymphangioma on perinatal ultrasound. Prenat Diagn 2003; 23: 763-765.

Chih-Ping Chen, Jin-Chung Shih, Shin-Lin Shih, Jon-Kway Huang, Jian-Pei Huang, Yi-Hui Lin, Wayseen Wang. Prenatal diagnosis of cephalothoracopagus janiceps disymmetros using three-dimensional power Doppler ultrasound and magnetic resonance imaging. Ultrasound Obstet Gynecol 2003; 22: 299-304.

Chih-Ping Chen, Shuan-Pei Lin. Distal 10q trisomy associated with bilateral hydronephrosis in infancy. Genet Couns 2003; 14: 359-362.

Chih-Ping Chen, Schu-Rern Chern, Dai-Dyi Town, Wayseen Wang, You-Wei Liao. Fetoplacental and fetoamniotic chromosomal discrepancies in prenatally detected mosaic trisomy 9. Prenat Diagn 2003; 23: 1019-1021.

Chih-Ping Chen. Second-trimester diagnosis of mosaic idic(20)(p11) confined to amniocytes without an abnormal phenotype. Genet Couns 2003; 14: 439-441.

Chih-Ping Chen. Prenatal imaging of the fetal anterior chest wall cystic hygroma by magnetic resonance imaging. Prenat Diagn 2003; 23: 1099-1100.

Chih-Ping Chen, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang, Chin-Yuan Tzen. Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy. Prenat Diagn 2004; 24: 19-25.

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Tung-Yao Chang, Wayseen Wang, Chin-Yuan Tzen. Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4. Prenat Diagn 2004; 24: 38-44.

Chih-Ping Chen, Chen-Chi Lee, Tung-Yao Chang, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis of mosaic distal 5p deletion and review of the literature. Prenat Diagn 2004; 24: 50-57.

Chih-Ping Chen, Jin-Chung Shih, Schu-Rern Chern, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin. Prenat Diagn 2004; 24: 63-66.

Chih-Ping Chen, Sho-Jen Cheng, Tung-Yao Chang, Li-Fan Yeh, Yi-Hui Lin, Wayseen Wang. Prenatal diagnosis of choledochal cyst using ultrasound and magnetic resonance imaging. Ultrasound Obstet Gynecol 2004; 23: 93-94.

Chih-Ping Chen, Tung-Yao Chang, Dai-Dyi Town, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang, Chin-Yuan Tzen. Partial trisomy 10 (10q11.2-->pter) and partial trisomy 18 (18p11.2-->pter) associated with abnormal sonographic findings and a maternal serum screen-positive result. Ultrasound Obstet Gynecol 2004; 23: 202-204.

Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Chin-Yuan Tzen, Chen-Chi Lee, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of the distal 11q deletion and review of the literature. Prenat Diagn 2004; 24: 130-136.

Chih-Ping Chen, Shuan-Pei Lin, Chin-Yuan Tzen, Fuu-Jen Tsai, Wuh-Liang Hwu, Wayseen Wang. Detection of a homozygous D645E mutation of the acid a-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II. Prenat Diagn 2004; 24: 231-232.

Chih-Ping Chen, Chin-Yuan Hsu. Prenatal identification of fetal radial aplasia and esophageal atresia in a pregnancy associated with polyhydramnios. Prenat Diagn 2004; 24: 232-234.

Chih-Ping Chen, Shuan-Pei Lin, Yuh-Ming Hwu, Tung-Yao Chang, Wayseen Wang. Prenatal identification of fetal overgrowth, abdominal wall defect, and neural tube defect in pregnancies achieved by assisted reproductive technology. Prenat Diagn 2004; 24: 396-398.

Chih-Ping Chen, Han-Yang Hung, Tung-Yao Chang, Shuan-Pei Lin, Wayseen Wang. Second-trimester nasal bone hypoplasia/ aplasia associated with cleidocranial dysplasia. Prenat Diagn 2004; 24: 399-400.

Chih-Ping Chen, Tung-Yao Chang, Yi-Hui Lin, Wayseen Wang. Prenatal sonographic diagnosis of acrania associated with amniotic bands. J Clin Ultrasound 2004; 32: 256-260.

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of interstitially satellited 6p. Prenat Diagn 2004; 24: 430-433.

Chih-Ping Chen, Schu-Rern Chern, Sho-Jen Cheng, Tung-Yao Chang, Li-Fan Yeh, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang, Chin-Yuan Tzen. Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature. Prenat Diagn 2004; 24: 455-462.

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Shuan-Pei Lin, Tung-Yao Chang, Wayseen Wang. Prenatal diagnosis of mosaic 22q11.2 microdeletion. Prenat Diagn 2004; 24: 660-662.

Chih-Ping Chen. Fetal mosaic trisomy 16 in association with elevated maternal serum free b-hCG. Prenat Diagn 2004; 24: 745-746.

Chih-Ping Chen, Chyi-Chyang Lin, Yueh-Chun Li, Schu-Rern Chern, Chen-Chi Lee, Wen-Lin Chen, Men-Shan Lee, Wayseen Wang, Chin-Yuan Tzen. Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature. Prenat Diagn 2004; 24: 767-773.

Chih-Ping Chen, Sho-Jen Cheng, Jin-Chern Sheu, Yi-Hui Lin. Third-trimester evaluation of choledochal cyst using magnetic resonance imaging. Prenat Diagn 2004; 24: 838-839.

Chih-Ping Chen, Shuan-Pei Lin. Detection of chromosome aberrations during prenatal genetic testing for single gene disorders. Prenat Diagn 2004; 24: 924-925.

Chih-Ping Chen, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis of complete trisomy 16q in two consecutive pregnancies. Prenat Diagn 2004; 24: 928-929.

Chih-Ping Chen, Chin-Yuan Hsu, Chen-Chi Lee, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of de novo pure partial monosomy 4p (4p15.1-->pter) in a growth-restricted fetus with a Greek warrior helmet face and unilateral facial cleft on three-dimensional ultrasound. Prenat Diagn 2004; 24: 934-936.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Chen-Chi Lee, Jon-Kway Huang, Wayseen Wang, You-Wei Liao. De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay. Genet Couns 2004; 15: 437-442.

Chih-Ping Chen, Chen-Chi Lee, Dai-Dyi Town, Meng-Shan Lee, Wayseen Wang. Discrepancy between the fetus and extra-embryonic tissues in prenatally detected mosaic distal 5p deletion. Genet Couns 2004; 15: 473-476.

Chih-Ping Chen. Perinatal identification of caudal regression syndrome and alobar holoprosencephaly in pregnancies with poor maternal metabolic control. Genet Couns 2004; 15: 485-488.

Chih-Ping Chen, Jin-Chern Sheu, Jon-Kway Huang, Yi-Hui Lin, Chin-Yuan Tzen, Wayseen Wang. Second-trimester magnetic resonance imaging of fetal sacrococcygeal teratoma with intrapelvic extension in a co-twin. Prenat Diagn 2004; 24: 1015-1017.

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Schu-Rern Chern, Wei-Min Chen, Chen-Chi Lee, Lie-Jiau Hsieh, Wayseen Wang. Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter). Prenat Diagn 2005; 25: 112-118.

Chih-Ping Chen, Yi-Ning Su, Chia-Cheng Hung, Chien-Nan Lee, Fon-Jou Hsieh, Tung-Yao Chang, Ming-Ren Chen, Wayseen Wang. Molecular genetic analysis of the TSC genes in two families with prenatally diagnosed rhabdomyomas. Prenat Diagn 2005; 25: 176-178.

Chih-Ping Chen, Yi-Ning Su, Jian-Pei Huang, Yi-Hui Lin, Wayseen Wang. Asymmetrical terminal limb defects in a hydropic infant with homozygous a-thalassemia-1. Prenat Diagn 2005; 25: 178-179.

Chih-Ping Chen, Jin-Chung Shih. Association of partial trisomy 9p and the Dandy-Walker malformation. Am J Med Genet 2005; 132A: 111-112.

Chih-Ping Chen, Schu-Rern Chern, Chen-Ju Lin, Chen-Chi Lee, Wayseen Wang, Chin-Yuan Tzen. A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly. Genet Couns 2005; 16: 49-57.

Chih-Ping Chen, Tung-Yao Chang, Chin-Yuan Tzen, Wayseen Wang, Chen-Chi Lee. Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1-->qter). Prenat Diagn 2005; 25: 263-264.

Chih-Ping Chen. Congenital malformations associated with maternal diabetes. Taiwan J Obstet Gynecol 2005; 44: 1-7.

Chih-Ping Chen, Chen-Ju Lin, Wayseen Wang, Taiwan Amniocentesis Collaborative Study Group. Impact of second-trimester maternal serum screening on prenatal diagnosis of Down syndrome and the use of amniocentesis in the Taiwanese population. Taiwan J Obstet Gynecol 2005; 44: 31-35.

Chih-Ping Chen, Chen-Yu Chen, Ching-Yi Lin, Sheng-Wen Shaw, Wayseen Wang, Chin-Yuan Tzen. Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes. Prenat Diagn 2005; 25: 264-266.

Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Ching-Yi Lin, Yi-Hui Lin, Wayseen Wang. A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error. Prenat Diagn 2005; 25: 327-330.

Chih-Ping Chen, Schu-Rern Chern, Chin-Yuan Hsu, Chen-Chi Lee, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis of de novo partial trisomy 13q (13q22 --> qter) and partial monosomy 8p (8p23.3 --> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart. Prenat Diagn 2005; 25: 334-336.

Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang, Hsiao-En Cindy Chen. Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency. Prenat Diagn 2005; 25: 383-389.

Chih-Ping Chen, Jin-Chung Shih, Chin-Yuan Tzen, Yi-Hui Lin, Wayseen Wang. Recurrent short-rib polydactyly syndrome: prenatal three-dimensional ultrasound findings and associations with congenital high airway obstruction and pyelectasia. Prenat Diagn 2005; 25: 417-418.

Chih-Ping Chen. Central nervous system anomalies associated with fetal trisomy 18. Prenat Diagn 2005; 25: 419-421.

Chih-Ping Chen. Omphalocele and congenital diaphragmatic hernia associated with fetal trisomy 18. Prenat Diagn 2005; 25: 421-423.

Chih-Ping Chen. Arthrogryposis of the wrist and ankle associated with fetal trisomy 18. Prenat Diagn 2005; 25: 423-425.

Deepak Kamnasaran, Chih-Ping Chen, Koenraad Devriendt, Lakshmi Mehta, Diane W. Cox. Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes. Genomics 2005; 85: 608-621.

Chih-Ping Chen, Schu-Rern Chern, Tzu-Hao Wang, Ding-Wei Hsueh, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang, Tsang-Ming Ko. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia. Prenat Diagn 2005; 25: 492-496.

Chih-Ping Chen, Schu-Rern Chern, Jin-Chern Sheu, Shuan-Pei Lin, Chin-Yuan Hsu, Tung-Yao Chang, Chen-Chi Lee, Wayseen Wang, Hsiao-En Cindy Chen. Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera. Prenat Diagn 2005; 25: 502-506.

Chih-Ping Chen, Sho-Jen Cheng, Yi-Hui Lin, Wayseen Wang. Prenatal imaging of limb-body wall complex by magnetic resonance imaging. Prenat Diagn 2005; 25: 521-523.

Chih-Ping Chen, Yu-Peng Liu, Jon-Kway Huang, Tung-Yao Chang, Ming-Ren Chen, Nan-Chang Chiu, Wayseen Wang. Contribution of ultrafast magnetic resonance imaging in prenatal diagnosis of sonographically undetected cerebral tuberous sclerosis associated with cardiac rhabdomyomas. Prenat Diagn 2005; 25: 523-524.

Chih-Ping Chen, Tung-Yao Chang, Shuan-Pei Lin, Jon-Kway Huang, Jeng-Daw Tsai, Nan-Chang Chiu, Wayseen Wang. Prenatal magnetic resonance imaging of Galloway-Mowat syndrome. Prenat Diagn 2005; 25: 525-527.

Chih-Ping Chen, Shuan-Pei Lin, Chen-Chi Lee, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Perinatal findings of partial trisomy 13q (13q14.1-->qter) resulting from paternal pericentric inversion of chromosome 13. Prenat Diagn 2005; 25: 527-528.

Ming Chen, Chih-Ping Chen, Jin-Chung Shih, Hung-Chieh Chou, Chia-Li Yu, Bao-Tyan Wang, Chang-Yao Hsieh. Antenatal treatment of chylothorax and cystic hygroma with OK-432 in nonimmune hydrops fetalis. Fetal Diagn Ther 2005; 20: 309-315.

Chih-Ping Chen. Acardiac twinning (twin reversed arterial perfusion sequence): a review of prenatal management. Taiwan J Obstet Gynecol 2005; 44: 105-115.

Chih-Ping Chen, Jin-Chung Shih, Tung-Yao Chang, Schu-Rern Chern, Ching-Yi Lin, Wayseen Wang, Chin-Yuan Tzen. Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy. Prenat Diagn 2005; 25: 618-620.

Chih-Ping Chen, Yu-Peng Liu, Shuan-Pei Lin, Jin-Cherng Sheu, Chin-Yuan Hsu, Tung-Yao Chang, Wayseen Wang. Prenatal magnetic resonance imaging demonstration of the systemic feeding artery of a pulmonary sequestration associated with in utero regression. Prenat Diagn 2005; 25: 721-723.

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Yen-Jiun Chen, Wayseen Wang. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2-->qter) and partial monosomy 5p (5p15.3-->pter). Prenat Diagn 2005; 25: 723-725.

Chih-Ping Chen, Jin-Chung Shih, Chin-Yuan Hsu, Chen-Yu Chen, Jon-Kway Huang, Wayseen Wang. Prenatal three-dimensional/four-dimensional sonographic demonstration of facial dysmorphisms associated with holoprosencephaly. J Clin Ultrasound 2005; 33: 312-318.

Yi-Hui Lin, Chih-Ping Chen, Sheng Chiang, Tze-Chien Chen. Ovarian abscess caused by nontyphoidal salmonella in a woman with systemic lupus erythematosus: a case report. J Reprod Med 2005; 50: 627-629.

Chih-Ping Chen. Fetal therapy and cytogenetic testing: prenatal detection of chromosome aberration during thoracocentesis for congenital chylothorax by karyotyping from pleural effusion fluid and review of the literature. Genet Couns 2005; 16: 301-305.

Chih-Ping Chen. Maternal diabetes and neural tube defects: prenatal diagnosis of lumbosacral myelomeningocele, ventriculomegaly, Arnold-Chiari malformation and foot deformities in a pregnancy with poor maternal metabolic control, and review of the literature. Genet Ccouns 2005; 16: 313-316.

Chih-Ping Chen, Chin-Yuan Hsu, Jon-Kway Huang, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of partial trisomy 16q and distal 22q13 deletion associated with dolichocephaly and frontal bossing on second-trimester ultrasound. Prenat Diagn 2005; 25: 964-966.

Ming Chen, Chih-Ping Chen, Jin-Chung Shih, Hung-Chieh Chou, Chia-Li Yu, Bao-Tyan Wang, Chang-Yao Hsieh. Antenatal treatment of chylothorax and cystic hygroma with OK-432 in nonimmune hydrops fetalis. Fetal Diagn Ther 2005; 20: 309-315.

Chia-Cheng Hung, Chien-Nan Lee, Chih-Ping Chen, Yuh-Jyh Jong, Chi-An Chen, Wen-Fang Cheng, Win-Li Lin, Yi-Ning Su. Quantification of relative gene dosage by single-base extension and high-performance liquid chromatography: application to the SMN1/SMN2 gene. Anal Chem 2005; 77: 6960-6968.

Ming-Chen, Jin-Chung Shih, Bao-Tyan Wang, Chih-Ping Chen, Chia-Li Yu. Fetal OK-432 pleurodesis: complete or incomplete? Ultrasound Obstet Gynecol 2005; 26: 791-793.

Hui-Ju Chen, Shuan-Pei Lin, Hung-Chang Lee, Chih-Ping Chen, Nan-Chang Chiu, Han-Yang Hung, Schu-Rern Chern, Chih-Kuang Chuang. Cystic fibrosis with homozygous R553X mutation in a Taiwanese child. J Hum Genet 2005; 50: 674-678.

Chih-Ping Chen, Schu-Rern Chern, Li-Feng Chen, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis. Prenat Diagn 2005; 25: 1067-1069.

Chih-Ping Chen, Schu-Rern Chern, Tung-Yao Chang, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of partial trisomy 10q (10q25.3-->qter) and partial monosomy 18q (18q23-->qter). Prenat Diagn 2005; 25: 1069-1071.

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Schu-Rern Chern, Chen-Chi Lee, Yen-Jiun Chen, Wayseen Wang. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter). Prenat Diagn 2005; 25: 1170-1172.

Chih-Ping Chen, Shuan-Pei Lin, Che-Sheng Ho, Schu-Rern Chern, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang. Distal 3p monosomy associated with epilepsy in a boy. Genet Couns 2005; 16: 429-432.

Chih-Ping Chen, Schu-Rern Chern, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Tzu-Hao Wang, Chen-Chi Lee, Chen-Wen Pan, Lie-Jiau Hsieh, Wayseen Wang. A paternally derived inverted duplication of distal 14q with a terminal 14q deletion. Am J Med Genet 2005; 139A: 146-150.

Jin-Chung Shih, Chih-Ping Chen. Spatio-temporal Image Correlation (STIC): Innovative 3D/4D Technique for Illustrating Unique and Independent Information and Diagnosing Complex Congenital Heart Diseases. Croat Med J 2005; 46: 812-820.

Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements. Prenat Diagn 2006; 26: 138-146.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Chyi-Chyang Lin, Yueh-Chun Li, Chen-Chi Lee, Lie-Jiau Hsieh, Wen-Lin Chen, Wayseen Wang. Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings. Prenat Diagn 2006; 26: 181-183.

Chih-Ping Chen, Schu-Rern Chern, Fang-Yu Hung, Ching-Yuan Hsu, Tung-Yao Chang, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Li-Feng Chen, Chin-Yuan Tzen, Wayseen Wang, Ryan Ma. Prenatal diagnosis of pure distal 18q deletion. Prenat Diagn 2006; 26: 184-185.

Chih-Ping Chen, Shuan-Pei Lin, Jin-Chern Sheu, Wayseen Wang, Chi-Yuan Tzen. Neonatal outcome of a prenatally detected 46,XX/46,XY true hermaphrodite. Prenat Diagn 2006; 26: 185-186.

Chih-Ping Chen, Yi-Ning Su, Shuan-Pei Lin, Mei-Ling Lin, Wayseen Wang. Favourable outcome in a pregnancy with concomitant maternal and fetal osteogenesis imperfecta associated with a novel COL1A2 mutation. Prenat Diagn 2006; 26: 188-190.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Jon-Kway Huang, Wayseen Wang. A cloverleaf skull associated with Crouzon syndrome. Arch Dis Child 2006; 91: F98.

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Jon-Kway Huang, Chen-Chi Lee, Wayseen Wang. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter). Genet Couns 2006; 17: 57-63.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Chen-Chi Lee, Li-Feng Chen, Yen-Jiun Chen, Wayseen Wang. Molecular cytogenetic analysis of de novo partial monosomy 4p (4p16.2-->pter) and partial trisomy 8p (8p23.2-->pter). Genet Couns 2006; 17: 81-85.

Chih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, Jeng-Daw Tsai, Jon-Kway Huang, Wayseen Wang. Recurrent Galloway-Mowat syndrome associated with abnormal prenatal sonographic findings. Genet Couns 2006; 17: 87-89.

Chih-Ping Chen, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Li-Feng Chen, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang. Detection of euchromatic variants and unusual C band heterochromatin variants at genetic amniocentesis. Genet Couns 2006; 17: 91-95.

Chih-Ping Chen, Schu-Rern Chern, Chyi-Chyang Lin, Tzu-Hao Wang, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Hui-Min Hua, Wayseen Wang. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter). Prenat Diagn 2006; 26: 313-320.

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Schu-Rern Chern, Chen-Chi Lee, Li-Feng Chen, Hui-Min Hua, Wayseen Wang. Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetus. Prenat Diagn 2006; 26: 387-391.

Chih-Ping Chen. Aplasia and duplication of the thumb and facial clefts associated with fetal trisomy 18. Am J Med Genet 2006; 140A: 960-963.

Chih-Ping Chen. Congenital heart defects associated with fetal trisomy 18. Prenat Diagn 2006; 26: 483-485.

Chih-Ping Chen, Yu-Peng Liu, Chin-Yuan Hsu, Shuan-Pei Lin, Wayseen Wang. Prenatal sonography and magnetic resonance imaging of pulmonary sequestration associated with a gastric duplication cyst. Prenat Diagn 2006; 26: 489-491.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Chen-Chi Lee, Jon-Kway Huang, Wayseen Wang. Direct transmission of the 18q– syndrome from mother to daughter. Genet Couns 2006; 17: 185-189.

Chih-Ping Chen, Shuan-Pei Lin, Chyi-Chyang Lin, Yann-Jang Chen, Schu-Rern Chern, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang. Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q. Am J Med Genet 2006; 140A: 1594-1600.

Hui-Ju Chen, Shuan-Pei Lin, Hung-Chang Lee, Chih-Ping Chen, Nan-Chang Chiu, Han-Yang Hung, Schu-Rern Chern, Chih-Kuang Chuang. Cystic fibrosis with homozygous R553X mutation in a Taiwanese child. J Hum Genet 2005; 50: 674-678.

Chih-Ping Chen, Yi-Ning Su, Chia-Cheng Hung, Jin-Chung Shih, Wayseen Wang. Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis. J Formos Med Assoc 2006; 105: 599-603.

Chih-Ping Chen, Tung-Yao Chang, Yi-Ning Su, Chin-Yuan Hsu, Wayseen Wang. Prenatal two- and three-dimensional ultrasound diagnosis of limb reduction defects associated with homozygous a-thalassemia. Fetal Diagn Ther 2006; 21: 374-379.

Chih-Ping Chen, Shuan-Pei Lin, Tzu-Hao Wang, Yann-Jang Chen, Ming Chen, Wayseen Wang. Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome. Prenat Diagn 2006; 26: 725-729.

Chih-Ping Chen, Tzu-Hao Wang, Schu-Rern Chern, Chin-Yuan Tzen, Chin-Yuan Hsu, Chen-Chi Lee, Li-Feng Chen, Chung-Chun Ma, Po-Tsang Chen, Wayseen Wang. Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2-->qter). Prenat Diagn 2006; 26: 752-755.

Chih-Ping Chen, Chyi-Chyang Lin, Tung-Yao Chang, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->ter-->qter). Prenat Diagn 2006; 26: 757-759.

Chih-Ping Chen, Chen-Li Lin, Li-Lu Chen, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis of mosaic ring chromosome 9. Prenat Diagn 2006; 26: 870-871.

Chih-Ping Chen, Shuan-Pei Lin, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang. Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl. Genet Couns 2006; 17: 301-306.

Chih-Ping Chen, Schu-Rern Chern, Pei-Yin Lee, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis of low-level mosaic trisomy 6 by amniocentesis. Prenat Diagn 2006; 26: 1093-1096.

Chih-Ping Chen, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Wayseen Wang. Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation. Fertil Steril 2006; 86: 1514e1-e2.

Chih-Ping Chen, Tzu-Hao Wang, Tung-Yao Chang, Chen-Chi Lee, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of the supernumerary der(22)t(11;22) syndrome associated with abnormal sonographic findings. Genet Couns 2006; 17: 469-472.

Chih-Ping Chen, Tzu-Hao Wang, Shuan-Pei Lin, Schu-Rern Chern, Ming-Ren Chen, Chen-Chi Lee, Yen-Jiun Chen, Wayseen Wang. 24 Mb deletion of 6q22.1-->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphism. Eur J Med Genet 2006; 49: 516-519.

Chen-Bin Wang, Shuan-Pei Lin, Chih-Ping Chen, Yen-Jiun Chen, Chen-Chi Lee. An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature. Genet Couns 2006; 17: 435-440.

Yi-Hui Lin, Chih-Ping Chen, Tze-Chien Chen, So-Jung Liang, Chun-Sen Hsu. Familial occurrence of isolated Dandy-Walker variant in two consecutive male fetuses. Genet Couns 2006; 17: 461-463.

Chia-Cheng Hung, Chih-Ping Chen, Shuan-Pei Lin, Shu-Chin Chien, Chien-Nan Lee, Wen-Fang Cheng, Wu-Shiun Hsieh, Ming S. Liu, Yi-Ning Su, Win-Li Lin. Quantitative assay of deletion or duplication genotype by capillary electrophoresis system: application in Prader–Willi syndrome and Duchenne Muscular Dystrophy. Clin Chem 2006; 52: 2203-2210.

Chin-Yuan Tzen, Bei-Liing Mau, Yu-Wen Huang, Ming-Jer Huang, Chih-Ping Chen. Is extramedullary plasmacytoma an oligoclonal tumour with clonal selection during tumour progression? Histopathology 2006; 48: 469-471.

Shin-Yu Lin, Shu-Chin Chien, Yi-Ning Su, Chien-Nan Lee, Chih-Ping Chen. Rapid genetic analysis of oculocutaneous albinism (OCA1) using denaturing high performance liquid chromatography (DHPLC) system. Prenat Diagn 2006; 26: 466-470.

Ming Chen, W-L Hwu, S-J Kuo, Chih-Ping Chen, P-L Yin, S-P Chang, D-J Lee, T-H Chen, B-T Wang, C-C Lin. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype. Ultrasound Obstet Gynecol 2006; 28: 939-943.

Chia-Cheng Hung, Yi-Ning Su, Shu-Chin Chien, Horng-Huei Liou, Chih-Chuan Chen, Pau-Chung Chen, Chia-Jung Hsieh, Chih-Ping Chen, Wang-Tso Lee, Win-Li Lin, Chien-Nan Lee. Molecular and clinical analyses of 84 patients with tuberous sclerosis complex. BMC Med Genet 2006; 7: 72.

Chih-Ping Chen, Shuan-Pei Lin, Chin-Yuan Tzen, Wuh-Liang Hwu, Schu-Rern Chern, Chih-Kuang Chuang, Shu-Shien Chiang, Wayseen Wang. Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome). Genet Couns 2007; 18: 49-56.

Chih-Ping Chen, Chen-Ju Lin, Tung-Yao Chang, Chin-Yuan Hsu, Chin-Yuan Tzen, Wayseen Wang. Second-trimester diagnosis of limb-body wall complex with literature review of pathogenesis. Genet Couns 2007; 18: 105-112.

Chih-Ping Chen. Chromosomal abnormalities associated with omphalocele. Taiwan J Obstet Gynecol 2007; 46: 1-8.

Chih-Ping Chen. Meckel syndrome: genetics, perinatal findings, and differential diagnosis. Taiwan J Obstet Gynecol 2007; 46: 9-14.

Chih-Ping Chen, Yu-Peng Liu, Shu-Chin Chien, Wayseen Wang. Prenatal diagnosis of concomitant gallbladder hydrops and pyelectasis with spontaneous resolution. Taiwan J Obstet Gynecol 2007; 46: 81-82.

Chih-Ping Chen, Chin-Yuan Hsu, Chin-Yuan Tzen, Schu-Rern Chern, Wayseen Wang. Prenatal diagnosis of pentalogy of Cantrell associated with hypoplasia of the right upper limb and ectrodactyly. Prenat Diagn 2007; 27: 86-87.

Chih-Ping Chen, Chen-Ju Lin, Tung-Yao Chang, Schu-Rern Chern, Chin-Yuan Tzen, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of the hypoplastic right heart syndrome with sex chromosome pentasomy (49,XXXXY). Prenat Diagn 2007; 27: 285-286.

Chih-Ping Chen, Tung-Yao Chang, Schu-Rern Chern, Chen-Chi Lee, Dai-Dyi Town, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis. Prenat Diagn 2007; 27: 383-385.

Chin-Yuan Hsu, Chih-Ping Chen, Chen-Ju Lin. An aberrant renal artery arising from the iliac artery imaged by three-dimensional power Doppler ultrasonography: a sign of fetal horseshoe kidney. Ultrasound Obstet Gynecol 2007; 29: 358-359.

Chih-Ping Chen, Tung-Yao Chang, Jon-Kway Huang, Wayseen Wang. Early second-trimester diagnosis of fetal otocephaly. Ultrasound Obstet Gynecol 2007; 29: 470-471.

Ming Chen, Chang-Yao Hsieh, Jin-Chung Shih, Chia-Hung Chou, Gwo-Chin Ma, Tze-Ho Chen, Tsung-Hsien Lee, Horng-Der Tsai, Alan D. Cameron, Chih-Ping Chen. Proinflammatory macrophage migratory inhibition factor and interleukin-6 are concentrated in pleural effusion of human fetuses with prenatal chylothorax. Prenat Diagn 2007; 27: 435-441.

Chih-Ping Chen, Chin-Yuan Hsu, Chin-Yuan Tzen, Chen-Chi Lee, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of mosaic ring chromosome 4. Prenat Diagn 2007; 27: 485-487.

Chih-Ping Chen. Syndromes and disorders associated with omphalocele (I): Beckwith-Wiedemann syndrome. Taiwan J Obstet Gynecol 2007; 46: 96-102.

Chih-Ping Chen. Syndromes and disorders associated with omphalocele (II): OEIS complex and pentalogy of Cantrell. Taiwan J Obstet Gynecol 2007; 46: 103-110.

Chih-Ping Chen. Syndromes and disorders associated with omphalocele (III): single gene disorders, neural tube defects, diaphragmatic defects and others. Taiwan J Obstet Gynecol 2007; 46: 111-120.

Chih-Ping Chen. Thoraco-omphalopagus conjoined twins associated with omphalocele and an umbilical cord cyst. Taiwan J Obstet Gynecol 2007; 46: 183-184.

Chih-Ping Chen. Prenatal diagnosis of atypical facial clefting should alert amniotic band syndrome and prompt a search for associated amniotic bands and other structural anomalies. Genet Couns 2007; 18: 255-257.

Chih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, Hung-Chang Lee, Han-Yang Hung, Hsiang-Yu Lin, Jian-Pei Huang, Wayseen Wang. Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome. J Clin Ultrasound 2007; 35: 409-412.

Chih-Ping Chen, Shu-Chin Chien, Schu-Rern Chern, Chin-Yuan Tzen, Wayseen Wang. Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies. Genet Couns 2007; 18: 343-347.

Chih-Ping Chen, Shuan-Pei Lin, Jeng-Daw Tsai, Jon-Kway Huang, Jui-Lung Yen, Ching-Chang Tseng, Wayseen Wang. Perinatal imaging findings of Galloway-Mowat syndrome. Genet Couns 2007; 18: 353-355.

Chih-Ping Chen. Prenatal diagnosis of arachnoid cysts. Taiwan J Obstet Gynecol 2007; 46: 187-198.

Chih-Ping Chen. Prenatal diagnosis of iniencephaly. Taiwan J Obstet Gynecol 2007; 46: 199-208.

Chih-Ping Chen, Tung-Yao Chang, Schu-Rern Chern, Wayseen Wang. Third-trimester 3D ultrasound evaluation of thanatophoric dysplasia type I. Taiwan J Obstet Gynecol 2007; 46: 281-283.

Chih-Ping Chen, Tung-Yao Chang, Yu-Peng Liu, Schu-Rern Chern, Wayseen Wang. Prenatal magnetic resonance imaging evaluation of a digynic triploid fetus. Taiwan J Obstet Gynecol 2007; 46: 284-285.

Hsiao-En Cindy Chen, Chih-Ping Chen, Chin-Yuan Hsu, Wayseen Wang. Typical body wall defect associated with craniofacial anomalies and amniotic bands diagnosed in early pregnancy. Taiwan J Obstet Gynecol 2007; 46: 286-287.

Chih-Ping Chen, Tzu-Hao Wang, Yann-Jang Chen, Tung-Yao Chang, Yu-Peng Liu, Chin-Yuan Tzen, Schu-Rern Chern, Wayseen Wang. Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1. Prenat Diagn 2007; 27: 967-969.

Chih-Ping Chen. Ruptured omphalocele with extracorporeal intestines mimicking gastroschisis in a fetus with Turner syndrome. Prenat Diagn 2007; 27: 1067-1068.

Chih-Ping Chen. Lethal multiple pterygium syndrome associated with omphalocele. Genet Couns 2007; 18: 451-453.

Chih-Ping Chen, Yi-Ning Su, Chyi-Chyang Lin, Yueh-Chun Li, Lie-Jiau Hsieh, Chen-Chi Lee, Wayseen Wang. Genetic counseling of prenatally detected unbalanced t(Y;15)(q12;p13). Genet Couns 2007; 18: 455-457.

Chih-Ping Chen, Fuu-Jen Tsai, Schu-Rern Chern, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang. Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p. Prenat Diagn 2007; 27: 1170-1173.

Chih-Ping Chen. Chromosomal abnormalities associated with neural tube defects (I): full aneuploidy. Taiwan J Obstet Gynecol 2007; 46: 325-335.

Chih-Ping Chen. Chromosomal abnormalities associated with neural tube defects (II): partial aneuploidy. J Obstet Gynecol 2007; 46: 336-351.

Chih-Ping Chen, Tung-Yao Chang, Wayseen Wang. Third-trimester ultrasound evaluation of arachnoid cysts. Taiwan J Obstet Gynecol 2007; 46: 427-428.

Chih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, Hsin-Tsung Ho. Abnormal prenatal hematological findings in congenital leukemia of Down syndrome with hepatosplenomegaly. Prenat Diagn 2007; 27: 1266-1267.

Chih-Ping Chen, Shu-Chin Chien, Hung-Hung Lin. Prenatal sonographic features of triploidy. J Med Ultrasound 2007; 15: 175-182.

Chih-Ping Chen, Shu-Chin Chien. Prenatal sonographic features of Turner syndrome. J Med Ultrasound 2007; 15: 251-257.

Wan-Yi Huang, Chia-Cheng Hung, Chien-Nan Lee, Yi-Ning Su, Chih-Ping Chen. Rapid prenatal diagnosis of Duchenne muscular dystrophy with gene duplications by ion-pair reversed-phase high-performance liquid chromatography coupled with competitive multiplex polymerase chain reaction strategy. Prenat Diagn 2007; 27: 653-656.

Wei-De Lin, Chang-Hai Tsai, Chih-Ping Chen, Fuu-Jen Tsai. Human gene mutations. Gene symbol: EXT2. Disease: exostoses (multiple) 2. Hum Genet 2007; 122: 211.

Wei-De Lin, Shuan-Pei Lin, Chih-Ping Chen, Fuu-Jen Tsai. Human gene mutations. Gene symbol: EXT1. Disease: exostoses (multiple) 1. Hum Genet 2007; 122: 212.

Wei-De Lin, Wuh-Liang Hwu, Su-Chiang Liu, Chih-Ping Chen, Fuu-Jen Tsai. Human gene mutations. Gene symbol: GLA. Disease: Fabry disease. Hum Genet 2007; 122: 212.

Chia-Cheng Hung, Chien-Nan Lee, Chih-Ping Chen, Yuh-Jyh Jong, Wu-Shiun Hsieh, Win-Li Lin, Yi-Ning Su, Su-Ming Hsu. Molecular assay of -α3.7 and -α4.2 deletions causing α-thalassemia by denaturing high-performance liquid chromatography. Clin Biochem 2007; 40: 817-821.

Chien-Liang Liu, Yuan-Ching Chang, Shih-Ping Cheng, Schu-Rern Chern, Tsen-Long Yang, Jie-Jen Lee, Ing-Cherng Guo, Chih-Ping Chen. The roles of serum leptin concentration and polymorphism in leptin receptor gene at codon 109 in breast cancer. Oncology 2007; 72: 75-81.

Lei Wan, Wei-Cheng Chen, Yuhsin Tsai, Yu-Tsun Kao, Yao-Yuan Hsieh, Cheng-Chun Lee, Chang-Hai Tsai, Chih-Ping Chen, Fuu-Jen Tsai. Growth hormone (GH) receptor C.1319 G>T polymorphism, but not exon 3 retention or deletion is associated with better first-year growth response to GH therapy in patients with GH deficiency. Pediatr Res 2007; 62: 735-740.

Cheng-Chun Lee, Wei-Yong Lin, Lei Wan, Yuhsin Tsai, Chang-Hai Tsai, Chung-Ming Huang, Chih-Ping Chen, Fuu-Jen Tsai. Association of interleukin-18 gene polymorphism with asthma in Chinese patients. J Clin Lab Anal 2008; 22: 39-44.

Chih-Ping Chen. Concomitant occurrence of holoprosencephaly and omphalocele. Genet Couns 2008; 19: 95-99.

Chih-Ping Chen, Yuh-Ming Hwu, Fuu-Jen Tsai, Wayseen Wang. Occipital encephalocele associated with iniencephaly mimicking a unilateral nuchal tumor on prenatal ultrasound. Genet Couns 2008; 19: 101-103.

Chih-Ping Chen, Edison Shieh, Schu-Rern Chern, Wayseen Wang. Triploidy and fetal holoprosencephaly. Genet Couns 2008; 19: 105-108.

Chih-Ping Chen, Yu-Peng Liu, Jian-Pei Huang, Tung-Yao Chang, Fuu-Jen Tsai, Jeng-DauTsai, Jin-Cherng Sheu, Wayseen Wang. Prenatal evaluation with magnetic resonance imaging of a giant blind ectopic ureter associated with a duplex kidney. Ultrasound Obstet Gynecol 2008; 31: 360-362.

Chih-Ping Chen. Syndromes, disorders and maternal risk factors associated with neural tube defects (I). Taiwan J Obstet Gynecol 2008; 47: 1-9.

Chih-Ping Chen. Syndromes, disorders and maternal risk factors associated with neural tube defects (II). Taiwan J Obstet Gynecol 2008; 47: 10-17.

Chih-Ping Chen, Tung-Yao Chang, Jeng-Hsiu Hung, Chen-Yu Chen, Wayseen Wang. Prenatal sonographic and magnetic resonance imaging demonstration of a right midline arachnoid cyst associated with ventriculomegaly, colpocephaly, dilation of the third ventricle, absence of cavum septi pellucidi, agenesis of the corpus callosum and mega cisterna magna. Taiwan J Obstet Gynecol 2008; 47: 91-92.

Chih-Ping Chen, Tung-Yao Chang, Hung-Hung Lin, Schu-Rern Chern, Wayseen Wang. Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy. Taiwan J Obstet Gynecol 2008; 47: 93-94.

Chih-Ping Chen, Jin-Chung Shih, Chin-Yuan Tzen, Schu-Rern Chern, Chen-Ju Lin, Wayseen Wang. Prenatal visualization of cebocephaly with a prominent nose in a second-trimester fetus with alobar holoprosencephaly and trisomy 13. Taiwan J Obstet Gynecol 2008; 47: 95-97.

Chih-Ping Chen, Yann-Jang Chen, Fuu-Jen Tsai, Schu-Rern Chern, Wayseen Wang. NFkB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 --> qter). Prenat Diagn 2008; 28: 364-365.

Chih-Ping Chen, Yann-Jang Chen, Schu-Rern Chern, Fuu-Jen Tsai, Tung-Yao Chang, Chen-Chi Lee, Dai-Dyi Town, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter). Prenat Diagn 2008; 28: 450-453.

Chih-Ping Chen, Tung-Yao Chang, Yu-Peng Liu, Fuu-Jen Tsai, Shu-Chin Chien, Chien-Ming Tsao, Hsiao-Bai Yang, Wayseen Wang. Prenatal 3-dimensional sonographic and MRI findings in omphalocele-exstrophy-imperforate anus-spinal defects complex. J Clin Ultrasound 2008; 36: 308-311.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Shu-Chin Chien, Fuu-Jen Tsai, Wayseen Wang. Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation. Genet Couns 2008; 19: 165-172.

Chih-Ping Chen, Shuan-Pei Lin, Fuu-Jen Tsai, Hung-Hung Lin, Schu-Rern Chern, Chih-Kuang Chuang, Chen-Chi Lee, Wayseen Wang. Transient abnormal myelopoiesis of mosaic trisomy 21 presenting fetoplacental cytogenetic discrepancy, hepatosplenomegaly, oligohydramnios and abnormal hematological findings. Genet Couns 2008; 19: 255-258.

Chih-Ping Chen, Shuan-Pei Lin, Fuu-Jen Tsai, Schu-Rern Chern, Wayseen Wang. Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation. Fertil Steril 2008; 89: 1826e5-e7.

Chih-Ping Chen. Syndromes, disorders and maternal risk factors associated with neural tube defects (III). Taiwan J Obstet Gynecol 2008; 47: 131-140.

Chih-Ping Chen. Syndromes, disorders and maternal risk factors associated with neural tube defects (IV). Taiwan J Obstet Gynecol 2008; 47: 141-150.

Chih-Ping Chen, Shuan-Pei Lin, Fuu-Jen Tsai, Schu-Rern Chern, Chen-Chi Lee, Wayseen Wang. A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay. Eur J Med Genet 2008; 51: 368-372.

Chih-Ping Chen, Yann-Jang Chen, Schu-Rern Chern, Fuu-Jen Tsai, Hung-Hung Lin, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele. Prenat Diagn 2008; 28: 865-867.

Chih-Ping Chen. Syndromes, disorders and maternal risk factors associated with neural tube defects (V). Taiwan J Obstet Gynecol 2008; 47: 259-266.

Chih-Ping Chen. Syndromes, disorders and maternal risk factors associated with neural tube defects (VI). Taiwan J Obstet Gynecol 2008; 47: 267-275.

Chih-Ping Chen. Syndromes, disorders and maternal risk factors associated with neural tube defects (VII). Taiwan J Obstet Gynecol 2008; 47: 276-282.

Chih-Ping Chen. Prenatal diagnosis, fetal surgery, recurrence risk and differential diagnosis of neural tube defects. Taiwan J Obstet Gynecol 2008; 47: 283-290.

Chih-Ping Chen, Shuan-Pei Lin, Fuu-Jen Tsai, Tzu-Hao Wang, Schu-Rern Chern, Wayseen Wang. Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review. Fertil Steril 2008; 90: 1198e11-e18.

Chih-Ping Chen, Tzu-Hao Wang, Chyi-Chyang Lin, Fuu-Jen Tsai, Lie-Jiau Hsieh, Wayseen Wang. Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system J Formos Med Assoc 2008; 107: 822-826.

Chih-Ping Chen, Fuu-Jen Tsai, Chen-Yu Chen, Hung-Hung Lin, Wayseen Wang. Limb-body wall complex with craniofacial defects after ovarian stimulation. Taiwan J Obstet Gynecol 2008; 47: 474-475.

Chih-Ping Chen, Chin-Yuan Tzen, Chen-Yu Chen, Fuu-Jen Tsai, Wayseen Wang. Concomitant exencepahly and limb defects associated with pentalogy of Cantrell. Taiwan J Obstet Gynecol 2008; 47: 476-477.

Chih-Ping Chen, Shu-Chin Chien. Prenatal sonographic features of 22q11.2 microdeletion syndrome. J Med Ultrasound 2008; 16: 123-129.

Wei-De Lin, Shuan-Pei Lin, Chung-Hsing Wang, Wuh-Liang Hwu, Chih-Kuang Chuang, Shio-Jean Lin, Yushin Tsai, Chih-Ping Chen, Fuu-Jen Tsai. Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patients. Clin Chim Acta 2008: 394; 89-93.

Ying-Ju Lin, Lei Wan, Jim Jinn-Chyuan Sheu, Chung-Ming Huang, Cheng-Wen Lin, Yu-Ching Lan, Chih-Ho Lai, Chien-Hui Hung, Yuhsin Tsai, Chang-Hai Tsai, T-H Lin, Chih-Ping Chen, Fuu-Jen Tsai. A/C polymorphism in the interleukin-18 coding region among Taiwanese systemic lupus erythematosus patients. Lupus 2008; 17: 124-127.

Sheng-Wen Shaw, Chih-Ping Chen, Po-Jen Cheng, Tzu-Hao Wang, Jia-Woei Hou, Cheng-Tao Lin, Shuenn-Dhy Chang, Hsiao-Lin Hwa, Ju-Li Lin, An-Shine Chao, Yung-Kuei Soong, Fon-Jou Hsieh. Gene dosage change of TPTE and BAGE2 and breakpoint analysis in Robertsonian Down syndrome. J Hum Genet. 2008; 53: 136-143.

Chia-Cheng Hung, Chien-Nan Lee, Chien-Hui Chang, Yuh-Jyh Jong, Chih-Ping Chen, Wu-Shiun Hsieh, Yi-Ning Su, Win-Li Lin. Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis. Clin Biochem 2008; 41: 162-166.

Kai-Chung Hsueh, Ying-Ju Lin, Jeng-Sheng Chang, Lei Wan, Yuhsin Tsai, Chang-Hai Tsai, Chih-Ping Chen, Fuu-Jen Tsai. Association of vascular endothelial growth factor C-634 G polymorphism in Taiwanese children with Kawasaki disease. Pediatr Cardiol 2008; 29: 292-296.

Yao-Yuan Hsieh, Da-Tian Bau, Chi-Chen Chang, Chang-Hai Tsai, Chih-Ping Chen, Fuu-Jen Tsai. XRCC4 codon 247*A and XRCC4 promoter -1394*T related genotypes but not XRCC4 intron 3 gene polymorphism are associated with higher susceptibility for endometriosis. Mol Reprod Dev 2008; 75: 946-951.

Sheng-Wen Shaw, Jenn-Jeih Hsu, Chien-Nan Lee, Ching-Hua Hsiao, Chih-Ping Chen, T'sang-T'ang Hsieh, Po-Jen Cheng. First- and second-trimester Down syndrome screening: current strategies and clinical guidelines. Taiwan J Obstet Gynecol 2008; 47: 157-162.

Pu-Tsui Wang, Shey-Chiang Su, Fang-Yu Hung, Shun-Long Weng, Chih-Ping Chen. Huge pelvic mass, cutaneous and vaginal fistulas, and bilateral hydronephrosis: a rare presentation of actinomycosis with a good response to conservative treatment and with long-term sequelae of renal atrophy and hydronephrosis. Taiwan J Obstet Gynecol 2008; 47: 206-221.

Kuang-Pin Hsu, Chih-Ping Chen, Shu-Chin Chien, Chin-Yuan Hsu. Hematocolpometra associated with an imperforate hymen and acute urinary retention mimicking a pelvic mass. Taiwan J Obstet Gynecol 2008; 47: 222-223.

Yu-Yueh Peng, Chih-Ping Chen, Shu-Chin Chien, Jen-Ruei Chen. Torsion of a huge ovarian cyst in a 90-year-old woman. Taiwan J Obstet Gynecol 2008; 47: 224-225.

Shwu-Shiuang Chen, Chih-Ping Chen, Shu-Chin Chien, Chin-Yuan Hsu. Spontaneous rupture of omental teratoma mimicking a ruptured ovarian teratoma. Taiwan J Obstet Gynecol 2008; 47: 229-232.

Hong-Ming Wu, Chih-Ping Chen, Kuo-Ming Chang, Shing-Jyh Chang. Omental trophoblastic implant with hemoperitoneum as a sequela of suction dilatation and curettage. Taiwan J Obstet Gynecol 2008; 47: 250-251.

Hung-Hung Lin, Ming-Chao Huang, Chen-Ju Lin, Chih-Ping Chen. Ectopic pregnancy with oral contraceptive use. Taiwan J Obstet Gynecol 2008; 47: 341-342.

Sheng-Wen Shaw, Po-Jen Cheng, Shuenn-Dhy Chang, Yu-Ting Lin, Chia-Cheng Hung, Chih-Ping Chen, Yi-Ning Su. Rapid prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography system. Acta Obstet Gynecol Scand 2008; 87: 960-968.

Yao-Yuan Hsieh, Chi-Chen Chang, Kung-Hao Hsu, Fuu-Jen Tsai, Chih-Ping Chen, Horng-Der Tsai. Effect of exercise training on calpain systems in lean and obese Zucker rats. Int J Biol Sci 2008; 4: 300-308.

Wei-De Lin, Chih-Ping Chen, D-Y Wang, Fuu-Jen Tsai. Gene symbol: LMX1B. Disease: Nail-patella syndrome Hum Genet 2008: 124: 295-296.

Chih-Ping Chen, Chin-Yuan Tzen, Schu-Rern Chern, Fuu-Jen Tsai, Chin-Yuan Hsu, Chen-Chi Lee, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang. A 12 Mb deletion of 6p24.1-->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys. Eur J Med Genet 2009; 52: 59-61.

Chih-Ping Chen. Placental abnormalities and preeclampsia in trisomy 13 pregnancies. Taiwan J Obstet Gynecol 2009; 48: 3-8.

Chih-Ping Chen, Fuu-Jen Tsai, Schu-Rern Chern, Tung-Yao Chang, Chin-Yuan Hsu, Hung-Hung Lin, Wayseen Wang. Prenatal diagnosis of 46,XX,der(13;21)(q10;q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites. Taiwan J Obstet Gynecol 2009; 48: 84-87.

Yu-Peng Liu, Chih-Ping Chen. Fetal MRI of hydrometrocolpos with septate vagina and uterus didelphys as well as massive urinary ascites due to cloacal malformation. Pediatr Radiol 2009; 39: 877.

Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations. Genet Couns 2009; 20: 281-288.

Chih-Ping Chen. Prenatal sonographic features of fetuses in trisomy 13 pregnancies (I). Taiwan J Obstet Gynecol 2009; 48: 210-217.

Chih-Ping Chen. Prenatal sonographic features of fetuses in trisomy 13 pregnancies (II). Taiwan J Obstet Gynecol 2009; 48: 218-224.

Chih-Ping Chen, Yu-Peng Liu, Fuu-Jen Tsai, Chen-Yu Chen, Hung-Hung Lin, Pei-Chen Wu, Wayseen Wang. Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review. Taiwan J Obstet Gynecol 2009; 48: 286-291.

Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Hung-Hung Lin, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism. Taiwan J Obstet Gynecol 2009; 48: 321-322.

Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Chin-Yuan Hsu, Kevin Ko, Wayseen Wang. Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly. Taiwan J Obstet Gynecol 2009; 48: 323-326.

Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Yu-Peng Liu, Fuu-Jen Tsai, Jonathan Kwei Hwang, Wayseen Wang. Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis. Taiwan J Obstet Gynecol 2009; 48: 327-331.

Chih-Ping Chen. Prenatal sonographic features of fetuses in trisomy 13 pregnancies (III). Taiwan J Obstet Gynecol 2009; 48: 342-349.

Chih-Ping Chen, Schu-Rern Chern, Pei-Chen Wu, Fuu-Jen Tsai, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Li-Feng Chen, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis. Taiwan J Obstet Gynecol 2009; 48: 389-399.

Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Shu-Shien Chiang, Chen-Chi Lee, Wayseen Wang. Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis. Taiwan J Obstet Gynecol 2009; 48: 403-407.

Chin-Yi Lin, Chih-Ping Chen, Chiung-Ling Liau, Pen-Hua Su, Teng-Fu Tsao, Tung-Yao Chang, Wayseen Wang. Prenatal diagnosis of monosomy 17p (17p13.3-->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly, and Miller-Dieker lissencephaly syndrome in a fetus. Taiwan J Obstet Gynecol 2009; 48: 408-411.

Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Wayseen Wang. Trisomy 13 mosaicism associated with cyclopia and cystic hygroma. Taiwan J Obstet Gynecol 2009; 48: 434-436.

Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Fuu-Jen Tsai, Jonathan Kwei Hwang, Wayseen Wang. 22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect: prenatal diagnosis by array comparative genomic hybridization. Taiwan J Obstet Gynecol 2009; 48: 437-440.

Chih-Ping Chen, Yi-Ning Su, Fuu-Jen Tsai, Hung-Hung Lin, Schu-Rern Chern, Meng-Shan Lee, Jonathan Kwei Hwang, Teresa Hsiao-Tien Chen, Wayseen Wang. Terminal 2q deletion and distal 15q duplication: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes. Taiwan J Obstet Gynecol 2009; 48: 441-445.

Chih-Ping Chen, Maw-Shuan Lee, Fuu-Jen Tsai, Ming-Chao Huang, Schu-Rern Chern, Wayseen Wang. Limb-body wall complex in one fetus of a dizygotic twin pregnancy conceived by egg donation, in vitro fertilization and embryo transfer: prenatal diagnosis and literature review. Taiwan J Obstet Gynecol 2009; 48: 446-450.

Chih-Ping Chen, Shu-Chin Chien. Prenatal sonographic features of Beckwith-Wiedemann syndrome. J Med Ultrasound 2009; 17: 98-106.

Yao-Yuan Hsieh, Chi-Chen Chang, Da-Tian Bau, Fuu-Jen Tsai, Chang-Hai Tsai, Chih-Ping Chen. The p21 codon 31*C- and DRD2 codon 313*T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma. Fertil Steril 2009; 91: 869-877.

Yung-Kuei Soong, Tzu-Hao Wang, Yun-Shien Lee, Chih-Ping Chen, Chia-Lin Chang, Szu-Ying Ho, An-Shine Chao, Po-Jen Cheng, Shuenn-Dyh Chang. Genome-wide detection of uniparental disomy in a fetus with intrauterine growth restriction using genotyping microarrays. Taiwan J Obstet Gynecol 2009; 48: 152-158.

Kai-Chung Hsueh, Ying-Ju Lin, Jeng-Sheng Chang, Lei Wan, Yu-Hsin Tsai, Chang-Hai Tsai, Chih-Ping Chen, Fuu-Jen Tsai. Association of interleukin-10 A-592C polymorphism in Taiwanese children with Kawasaki disease. J Korean Med Sci 2009; 24: 438-442.

Ming Chen, Hsiang-Hsu Kuo, Yi-Chen Huang, Yu-Yuan Ke, Shun-Ping Chang, Chih-Ping Chen, Dong-Jay Lee, Meng-Luen Lee, Mei-Hui Lee, Tze-Ho Chen, Chia-Hsiang Chen, Hui-Mei Lin, Chin-San Liu, Gwo-Chin Ma. A case of restrictive dermopathy with complete chorioamniotic membrane separation caused by a novel homozygous nonsense mutation in the ZMPSTE24 gene. Am J Med Genet 2009; 149A: 1550-1554.

Tzong-Yuan Wu, Chih-Ping Chen. Dual action of memantine in Alzheimer disease: a hypothesis. Taiwan J Obstet Gynecol 2009; 48: 273-277.

Shu-Chin Chien, Chih-Ping Chen, Chyi-Chyang Lin, Li-Chia Huang, Cheng-Tiao Hsieh, Fuu-Jen Tsai. Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and a literature review. Taiwan J Obstet Gynecol 2009; 48: 292-295.

Chia-Cheng Hung, Shin-Yu Lin, Shuan-Pei Lin, Dou-Ming Niu, Ni-Chung Lee, Wen-Fang Cheng, Chih-Ping Chen, Win-Li Lin, Chien-Nan Lee, Yi-Ning Su. Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR. Electrophoresis 2009; 30: 410-416.

Chen C-H, Chen T-H, Kuo S-J, Chih-Ping Chen, Lee D-J, Ke Y-Y, Yeh K-T, Ma G-C, Liu C-S, Shih J-C, Chen M. Genetic evaluation and management of fetal chylothorax: review and insights from a case of Noonan syndrome. Lymphology 2009; 42: 134-138.

Chia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, Hui-Yu Cheng, Shuan-Pei Lin, Ming-Ren Chen, Chih-Ping Chen, Chien-Hui Chang, Chiou-Ya Lin, Chih-Chieh Yu, Hsin-Hui Chiu, Wen-Fang Cheng, Hong-Nerng Ho, Dau-Ming Niu, Yi-Ning Su. Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome. Ann Hum Genet 2009; 73: 559-567.

Tsung-Hsien Su, Wen-Chu Huang, Mei-Yu Lee, Tzu-Yin Lin, Hui-Chin Chang, Chih-Ping Chen. Tension-free vaginal tape-obturator procedure for treatment of severe urodynamic stress incontinence: Subjective and objective outcomes during 2 years of follow-up. J Obstet Gynecol Res 2009; 35:1077-1082.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Fuu-Jen Tsai, Tao-Yeuan Wang, Hung-Hung Lin, Wayseen Wang. Prenatal diagnosis of X-linked myotubular myopathy. Prenat Diagn 2010; 30: 177-179.

Chih-Ping Chen. Prenatal sonographic features of fetuses in trisomy 13 pregnancies (IV). Taiwan J Obstet Gynecol 2010; 49: 3-12.

Chih-Ping Chen. Prenatal diagnosis and genetic counseling for mosaic trisomy 13. Taiwan J Obstet Gynecol 2010; 49: 13-22.

Chih-Ping Chen, Schu-Rern Chern, Pei-Chen Wu, Fuu-Jen Tsai, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Li-Feng Chen, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang. Unbalanced and balanced heterologous acrocentric rearrangement involving chromosome 21 at amniocentesis. Taiwan J Obstet Gynecol 2010; 49: 62-68.

Chih-Ping Chen, Yu-Peng Liu, Shuan-Pei Lin, Ming Chen, Fuu-Jen Tsai, Yu-Ting Chen, Li-Feng Chen, Jonathan Kwei Hwang, Wayseen Wang. Ventriculomegaly, intrauterine growth restriction, and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2 --> pter) in a fetus. Taiwan J Obstet Gynecol 2010; 49: 81-86.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Chin-Yuan Hsu, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21 --> q11.23 by array comparative genomic hybridization. Taiwan J Obstet Gynecol 2010; 49: 117-119.

Chih-Ping Chen, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Chin-Yuan Hsu, Ming-Chao Huang, Wayseen Wang. Rapid genome-wide aneuploidy diagnosis using uncultured amniocytes and array comparative genomic hybridization in pregnancy with abnormal ultrasound findings detected in late second and third trimesters. Taiwan J Obstet Gynecol 2010; 49: 120-123.

Chih-Ping Chen, Yi-Ning Su, Chin-Yuan Hsu, Fuu-Jen Tsai, Shu-Chin Chien, Schu-Rern Chern, Meng-Shan Lee, Pei-Chen Wu, Hsaio-En Cindy Chen, Wayseen Wang. Abnormally flat facial profile on two- and three-dimensional ultrasound and array comparative genomic hybridization for the diagnosis of Pallister-Killian syndrome. Taiwan J Obstet Gynecol 2010; 49: 124-128.

Chih-Ping Chen, Yi-Ning Su, Chin-Yuan Hsu, Pei-Ying Ling, Fuu-Jen Tsai, Schu-Rern Chern, Pei-Chen Wu, Hsaio-En Cindy Chen, Wayseen Wang. Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18. Taiwan J Obstet Gynecol 2010; 49: 129-132.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Li-Feng Chen, Meng-Shan Lee, Wayseen Wang. Deletion 2q37.3->qter and duplication 15q24.3->qter characterized by array CGH in a girl with epilepsy and dysmorphic features. Genet Couns 2010; 21: 263-267.

Chih-Ping Chen. Pathophysiology of increased fetal nuchal translucency thickness. Taiwan J Obstet Gynecol 2010; 49: 133-138.

Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, Fuu-Jen Tsai, Yu-Ting Chen, Schu-Rern Chern, Chen-Chi Lee, Dai-Dyi Town, Li-Feng Chen, Pei-Chen Wu, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18. Taiwan J Obstet Gynecol 2010; 49: 188-191.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Tao-Yeuan Wang, Fuu-Jen Tsai, Hung-Hung Lin, Pei-Chen Wu, Wayseen Wang. Detection and comparison of the cytomegalovirus DNA levels in amniotic fluid and fetal ascites in a second-trimester fetus with massive ascites, hyperechogenic bowel, ventriculomegaly and intrauterine growth restriction. Taiwan J Obstet Gynecol 2010; 49: 206-210.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Chen-Yu Chen, Fuu-Jen Tsai, Yu-Peng Liu, Schu-Rern Chern, Pei-Chen Wu, Hsaio-En Cindy Chen,Wayseen Wang. Apert syndrome associated with upper airway obstruction and gastroesophageal reflux including polyhydramnios in the third trimester. Taiwan J Obstet Gynecol 2010; 49: 231-234.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Hsaio-En Cindy Chen, Shu-Shien Chiang, Wayseen Wang. Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation. Taiwan J Obstet Gynecol 2010; 49: 235-238.

Chih-Ping Chen, Schu-Rern Chern, Chia-Hsun Wu, Fuu-Jen Tsai, Pei-Chen Wu, Wayseen Wang. Detection of a balanced homologous acrocentric rearrangement rea(14q14q) and low-grade X-chromosome mosaicism in a couple with repeated pregnancy losses. Taiwan J Obstet Gynecol 2010; 49: 239-242.

Chih-Ping Chen, Yi-Ning Su, Jon-Kway Huang, Yu-Peng Liu, Fuu-Jen Tsai, Chun-Kuang Yang, Jian-Pei Huang, Chen-Yu Chen, Pei-Chen Wu, Wayseen Wang. Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome. Taiwan J Obstet Gynecol 2010; 49: 243-246.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Yann-Jang Chen, Fuu-Jen Tsai, Pei-Chen Wu, Wayseen Wang. Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-->q24.3 in a girl with autistic features and developmental delay. Eur J Med Genet 2010; 53: 217-220.

Chih-Ping Chen, Fuu-Jen Tsai, Chen-Chi Lee, Wen-Lin Chen, Chen-Wen Pan, Pei-Chen Wu, Wayseen Wang. Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q. Genet Couns 2010; 21: 353-357.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Wayseen Wang. A de novo 7.9 Mb deletion in 22q13.2→qter in a boy with autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findings. Eur J Med Genet 2010; 53: 329-332.

Chih-Ping Chen, Ming Chen, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Chin-Yuan Hsu, Pei-Chen Wu, Dai-Dyi Town, Dong-Jay Lee, Gwo-Chin Ma, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly. Taiwan J Obstet Gynecol 2010; 49: 320-326.

Chih-Ping Chen, Yung-Ting Guo, Shuan-Pei Lin, Yi-Ning Su, Yann-Jang Chen, Rui-Yuan Hseuh, Yi-Hui Lin, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Wayseen Wang. Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization. Taiwan J Obstet Gynecol 2010; 49: 327-332.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Yu-Ming Hwu, Shuan-Pei Lin, Chyong-Hsin Hsu, Fuu-Jen Tsai, Tao-Yeuan Wang, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Li-Feng Chen, Wayseen Wang. Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses. Taiwan J Obstet Gynecol 2010; 49: 333-340.

Chih-Ping Chen, Hsien-Ming Lin, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang. Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses. Taiwan J Obstet Gynecol 2010; 49: 341-350.

Chih-Ping Chen, Chyi-Chyang Lin, Tsang-Ming Ko, Fuu-Jen Tsai, Schu-Rern Chern, Chen-Chi Lee, Yu-Ting Chen, Pei-Chen Wu, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21. Taiwan J Obstet Gynecol 2010; 49: 377-380.

Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Chen-Chi Lee, Wen-Ling Chen, Li-Feng Chen, Pei-Chen Wu, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22. Taiwan J Obstet Gynecol 2010; 49: 381-384.

Chih-Ping Chen, Yu-Peng Liu, Tung-Yao Chang, Fuu-Jen Tsai, Chen-Yu Chen, Pei-Chen Wu, Teresa Hsiao-Tien Chen, Wayseen Wang. Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy. Taiwan J Obstet Gynecol 2010; 49: 385-386.

Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Yu-Peng Liu, Fuu-Jen Tsai, Ming-Ren Chen, Jonathan Kwei Hwang, Teresa Hsiao-Tien Chen, Wayseen Wang. Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene. Taiwan J Obstet Gynecol 2010; 49: 387-389.

Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Hung-Hung Lin, Pei-Chen Wu, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis of partial monosomy 1q (1q42.3→ qter) associated with hydrocephalus and corpus callosum agenesis Genet Couns 2010; 21: 451-455.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Fuu-Jen Tsai, Chen-Chi Lee, Chen-Wen Pan, Pei-Chen Wu, Wayseen Wang. A 5.3-Mb duplication of 9p12 --> p13.1 characterized by array CGH in a female infant with developmental delay. Genet Couns 2010; 21: 457-460.

Shih-Jung Cheng, Pei-Hao Chen, Lu-An Chen, Chih-Ping Chen. Stroke during pregnancy and puerperium: clinical perspectives. Taiwan J Obstet Gynecol 2010; 49: 395-400.

Chih-Ping Chen, Pei-Chen Wu, Chen-Ju Lin, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Li-Feng Chen, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang. Balanced reciprocal translocations detectred at amniocentesis. Taiwan J Obstet Gynecol 2010; 49: 455-467.

Chih-Ping Chen, Ming Chen, Yi-Ning Su, Chin-Yuan Hsu, Fuu-Jen Tsai, Schu-Rern Chern, Pei-Chen Wu, Chen-Chi Lee, Wayseen Wang. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings. Taiwan J Obstet Gynecol 2010; 49: 473-480.

Chih-Ping Chen, Yi-Ning Su, Chin-Yuan Hsu, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Po-Tsang Chen, Wayseen Wang. Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling. Taiwan J Obstet Gynecol 2010; 49: 481-486.

Chih-Ping Chen, Ming-Chou Chiang, Tzu-Hao Wang, Chuen Hsueh, Shueen-Dyh Chang, Fuu-Jen Tsai, Chao-Ning Wang, Schu-Rern Chern, Wayseen Wang. Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea. Taiwan J Obstet Gynecol 2010; 49: 487-494.

Chih-Ping Chen, Ming Chen, Tsang-Ming Ko, Gwo-Chin Ma, Fuu-Jen Tsai, Ming-Song Tsai, Pei-Chen Wu, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8. Taiwan J Obstet Gynecol 2010; 49: 500-505.

Chih-Ping Chen, Yi-Ning Su, Richard Shih-Hung Young, Fuu-Jen Tsai, Pei-Chen Wu, Schu-Rern Chern, Dai-Dyi Town, Chen-Wen Pan, Wayseen Wang. Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31 →qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization. Taiwan J Obstet Gynecol 2010; 49: 506-512.

Chih-Ping Chen, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Chin-Yuan Hsu, Pei-Chen Wu, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang. Partial trisomy 10q (10q25.1 →qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization. Taiwan J Obstet Gynecol 2010; 49: 539-543.

Chih-Ping Chen, Ming-Chao Huang, Yi-Ning Su, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Dai-Dyi Town, Chen-Wen Pan, Wayseen Wang. Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling. Taiwan J Obstet Gynecol 2010; 49: 544-547.

Chih-Ping Chen, Shu-Chin Chien. Prenatal sonographic features of Pallister-Killian syndrome. J Med Ultrasound 2010; 18: 43-53.

Chih-Ping Chen, Shu-Chin Chien. Prenatal sonographic features of Miller-Dieker syndrome. J Med Ultrasound 2010; 18: 147-152.

Sheng-Wen Steven Shaw, Shin-Yu Lin, Chia-Hui Lin, Yi-Ning Su, Po-Jen Cheng, Chien-Nan Lee, Chih-Ping Chen. Second-trimester maternal serum quadruple test for Down syndrome screening: a Taiwanese population-based study. Taiwan J Obstet Gynecol 2010; 49: 30-34.

Chao-Lan Shih, Yao-Ching Hung, Chih-Ping Chen, Shu-Chin Chien, Wu-Chou Lin. Resectoscopic excision of the vaginal septum in a virgin with uterus didelphys and obstructed unilateral vagina. Taiwan J Obstet Gynecol 2010; 49: 109-111.

Fang-Yu Hung, Pu-Tsui Wang, Shun-Long Weng, Chih-Ping Chen. Placenta percreta presenting as a pinhole uterine rupture and acute abdomen. Taiwan J Obstet Gynecol 2010; 49: 115-116.

Yu-Peng Liu, Chih-Ping Chen, Shin-Lin Shih, Yi-Fang Chen, Fei-Shih Yang, Su-Chiu Chen. Fetal cystic lung lesions: Evaluation with magnetic resonance imaging. Pediatr Pulmonol 2010; 45: 592-600.

Hsiao-Chen Tu, Chih-Ping Chen, Wen-Hsiung Chan. Epicatechin gallate decreases the viability and subsequent embryonic development of mouse blastocysts. Taiwan J Obstet Gynecol 2010; 49: 174-180.

Hui-Ju Lin, Yu-Chuen Huang, Jane-Ming Lin, Jer-Yuarn Wu, Liuh-An Chen, Chao-Jen Lin, Yung-Ping Tsui, Chih-Ping Chen, Fuu-Jen Tsai. Single-nucleotide polymorphisms in chromosome 3p14.1- 3p14.2 are associated with susceptibility of type 2 diabetes with cataract. Mol Vis 2010; 16: 1206-1214.

Yu-Chuen Huang, Y-J Lin, J-S Chang, S-Y Chen, Lei Wan, Jim Jinn-Chyuan Sheu, Chih-Ho Lai, Wei-Yong Lin, Hsing-Ping Liu, Chih-Ping Chen, Fuu-Jen Tsai. Single nucleotide polymorphism rs2229634 in the ITPR3 gene is associated with the risk of developing coronary artery aneurysm in children with Kawasaki disease. Int J Immunogenet 2010; 37: 439-443.

Tzong-Yuan Wu, Chih-Ping Chen, Tzyy-Rong Jinn. Alzheimer's disease: Aging, insomnia and epigenetics. Taiwan J Obstet Gynecol 2010; 49: 468-472.

Hsiang-Yu Lin, Ming-Ren Chen, Ching-Chi Lin, Chih-Ping Chen, Dar-Shong Lin, Chih-Kuang Chuang, Dau-Ming Niu, Jui-Hung Chang, Hung-Chang Lee, Shuan-Pei Lin. Polysomnographic characteristics in patients with mucopolysaccharidoses. Pediatr Pulmonol 2010; 45: 1205-1212.

Hsiang-Yu Lin, Ming-Ren Chen, Chih-Kuang Chuang, Chih-Ping Chen, Dar-Shong Lin, Yin-Hsiu Chien, Yu-Yuan Ke, Fuu-Jen Tsai, Hui-Ping Pan, Shio-Jean Lin, Wuh-Liang Hwu, Dau-Ming Niu, Ni-Chung Lee, Shuan-Pei Lin. Enzyme replacement therapy for mucopolysaccharidosis VI-experience in Taiwan. J Inherit Metab Dis 2010; PMID: 20924685.

Chih-Ping Chen, Shuan-Pei Lin, Fuu-Jen Tsai, Schu-Rern Chern, Pei-Chen Wu, Chen-Chi Lee, Meng-Shan Lee, Yu-Ting Chen, Wayseen Wang. Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome. Genet Couns 2011; 22: 79-83.

Chih-Ping Chen, Pei-Chen Wu, Chen-Ju Lin, Schu-Rern Chern, Fuu-Jen Tsai, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Li-Feng Chen, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang. Unbalanced reciprocal translocations at amniocentesis. Taiwan J Obstet Gynecol 2011; 50: 48-57.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Chin-Yuan Hsu, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Meng-Shan Lee, Wayseen Wang. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization. Taiwan J Obstet Gynecol 2011; 50: 67-73.

Chih-Ping Chen, Yi-Ning Su, Shin-Yu Lin, Chih-Long Chang, Yeou-Lih Wang, Jiau-Pei Huang, Chen-Yu Chen, Fang-Yu Hung, Yi-Yung Chen, Pei-Chen Wu, Wayseen Wang. Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations. Taiwan J Obstet Gynecol 2011; 50: 85-94.

Chih-Ping Chen, Tao-Yeuan Wang, Pei-Chen Wu, Fuu-Jen Tsai, Wayseen Wang. Pathological characterization of a malformed umbilical cord associated with body stalk anomaly. Taiwan J Obstet Gynecol 2011; 50: 126-128.

Chih-Ping Chen, Yau-Kun Kuo, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Yu-Ting Chen, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10) del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly. Taiwan J Obstet Gynecol 2011; 50: 182-187.

Chih-Ping Chen, Ming Chen, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Pei-Chen Wu, Wen-Lin Chen, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4. Taiwan J Obstet Gynecol 2011; 50: 188-195.

Chih-Ping Chen, Yi-Ning Su, Fuu-Jen Tsai, Ming-Huei Lin, Pei-Chen Wu, Schu-Rern Chern, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang. Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization. Taiwan J Obstet Gynecol 2011; 50: 205-211.

Chih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, Jeng-Daw Tsai, Chen-Yu Chen, Shin-Lin Shih, Fuu-Jen Tsai, Pei-Chen Wu, Wayseen Wang. Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findings. Taiwan J Obstet Gynecol 2011; 50: 212-216.

Chih-Ping Chen, Jui-Der Liou, Chi-Hsin Chiang, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Yu-Ting Chen, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis. Taiwan J Obstet Gynecol 2011; 50: 245-248.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p. Taiwan J Obstet Gynecol 2011; 50: 249-252.

Chih-Ping Chen, Ming Chen, Gwo-Chin Ma, Shun-Ping Chang, Yi-Yung Chen, Pei-Chen Wu, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome. Taiwan J Obstet Gynecol 2011; 50: 253-257.

Chih-Ping Chen, Chin-Yuan Hsu, Pei-Chen Wu, Fuu-Jen Tsai, Wayseen Wang. Prenatal ultrasound demonstration of limb-body wall complex with megacystis. Taiwan J Obstet Gynecol 2011; 50: 258-260.

Schu-Rern Chern, Sheng-Hsiang Li, Chien-Ling Chiu, Hsiao-Ho Chang, Chih-Ping Chen, Edmund I Tsuen Chen. Spatiotemporal expression of SERPINE2 in the human placenta and its role in extravillous trophoblast migration and invasion. Reprod Biol Endocrinol 2011; 9: 106.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Li-Feng Chen,Wayseen Wang. A 24.2-Mb deletion of 4q12-->q21.21 characterized by array CGH in a 13½-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed puberty. Genet Couns 2011; 22: 255-261.

Chih-Ping Chen, Shuan-Pei Lin, Ming Chen, Yi-Ning Su, Schu-Rern Chern, Tao-Yeuan Wang, Yu-Peng Liu, Fuu-Jen Tsai, Chen-Chi Lee, Yen-Jiun Chen, Wayseen Wang. Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses. Genet Couns 2011; 22: 273-280.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Wayseen Wang. Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delay. Genet Couns 2011; 22: 321-326.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Wen-Lin Chen, Wayseen Wang. Self-injurious behavior associated with trisomy 9p (9p13.1-->p24.3). Genet Couns 2011; 22: 327-331.

Chen-Ju Lin, Shu-Chin Chien, Chih-Ping Chen. The use of misoprostol in termination of second-trimester pregnancy. Taiwan J Obstet Gynecol 2011; 50: 275-282.

Chih-Ping Chen, Ming Chen, Yi-Ju Pan, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Yu-Ting Chen, Wayseen Wang. Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review. Taiwan J Obstet Gynecol 2011; 50: 331-338.

Chih-Ping Chen, Yi-Ning Su, Hung-Hung Lin, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Wayseen Wang. De novo duplication of Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure. Taiwan J Obstet Gynecol 2011; 50: 339-344.

Chih-Ping Chen, Yi-Ning Su, Yi-Yung Chen, Schu-Rern Chern, Yu-Peng Liu, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Wayseen Wang. Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia and intrauterine growth restriction. Taiwan J Obstet Gynecol 2011; 50: 345-352.

Chih-Ping Chen, Yi-Hui Lin, Heng-Kien Au, Chin-Yuan Hsu, Yu-Peng Liu, Pei-Chen Wu, Schu-Rern Chern, Yu-Ting Chen, Li-Feng Chen, Adam Hwa-Ming Hsieh, Wayseen Wang. Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3). Taiwan J Obstet Gynecol 2011; 50: 359-365.

Chih-Ping Chen, Yi-Ning Su, Shin-Yu Lin, Schu-Rern Chern, Yu-Ting Chen, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction. Taiwan J Obstet Gynecol 2011; 50: 390-393.

Chih-Ping Chen, Yi-Ning Su, Ming Chen, Jain-Pei Huang, Fuu-Jen Tsai, Pei-Chen Wu, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation. Taiwan J Obstet Gynecol 2011; 50: 394-398.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Pei-Chen Wu, Wayseen Wang. Prenatal diagnosis of microvillus inclusion disease. Taiwan J Obstet Gynecol 2011; 50: 399-400.

Chih-Ping Chen, Yi-Ning Su, Yu-Ting Chen, Wen-Lin Chen, Lee James Hsu, Wayseen Wang. Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene. Taiwan J Obstet Gynecol 2011; 50: 401-404.

Chih-Ping Chen, Yi-Ning Su, Pei-Chen Wu, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang. Rapid aneuploidy diagnosis by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal nuchal edema and mild ascites. J Med Ultrasound 2011; 19: 64-67.

Chih-Ping Chen, Yi-Ning Su, Chin-Yuan Hsu, Ming-Ren Chen, Yu-Peng Liu, Pei-Chen Wu, Wayseen Wang. Prenatal diagnosis of cerebral tubers by magnetic resonance imaging following detection of cardiac rhabdomyomas by prenatal ultrasound in a fetus with a nonsense mutation in the TSC2 gene. J Med Ultrasound 2011; 19: 68-70.

Chih-Ping Chen, Yi-Yung Chen, Jun-Wei Su, Wayseen Wang. Prenatal diagnosis of limbebody wall complex with craniofacial defects. J Med Ultrasound 2011; 19: 112-114.

Chih-Ping Chen, Jeng-Daw Tsai, Chin-Yuan Hsu, Tung-Yao Chang, Yu-Peng Liu, Jun-Wei Su, Wayseen Wang. Perinatal magnetic resonance imaging demonstration of duplication of the right renal collecting system with ipsilateral hydronephrosis and hydroureter, and contralateral renal hypoplasia. J Med Ultrasound 2011; 19: 143-145.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Fuu-Jen Tsai, Meng-Shan Lee, Yen-Jiun Chen, Wayseen Wang. Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and mental retardation. Genet Couns 2011; 22: 425-430.

Chih-Ping Chen, Ling-Yuh Kao, Yi-Ning Su, Ming Chen, Shueen-Dyh Chang, Wayseen Wang. A 20.5-Mb germline deletion of 13q13.1-->q14.3 and somatic mutations of the RB1 gene in an 8-year-old girl with unilateral retinoblastoma, developmental delay and mental retardation. Genet Couns 2011; 22: 431-434.

Chih-Ping Chen, Chin-Yuan Hsu, Jun-Wei Su, Hsiao-En Cindy Chen, Alan Hwa-Ruey Hsieh, Alex Hwa-Jiun Hsieh, Wayseen Wang. Conjoined twins detected in the first trimester: a review. Taiwan J Obstet Gynecol 2011; 50: 424-431.

Chih-Ping Chen, Schu-Rern Chern, Chen-Yu Chen, Pei-Chen Wu, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang. Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of left wrist and aplasia of left thumb. Taiwan J Obstet Gynecol 2011; 50: 479-484.

Chih-Ping Chen, Yi-Ning Su, Chin-Yuan Hsu, Schu-Rern Chern, Chen-Chi Lee, Yu-Ting Chen, Wen-Lin Chen, Wayseen Wang. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy. Taiwan J Obstet Gynecol 2011; 50: 485-491.

Chih-Ping Chen, Hsu-Kuaing Huang, Pei-Ying Lin, Yi-Ning Su, Ming Chen, Fuu-Jen Tsai, Pei-Chen Wu, Schu-Rern Chern, Yu-Ting Chen, Chen-Chi Lee, Wayseen Wang. A de novo duplication of chromosome 21q22.11-->qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings. Taiwan J Obstet Gynecol 2011; 50: 492-498.

Chih-Ping Chen, Yi-Ning Su, Yi-Yung Chen, Jun-Wei Su, Schu-Rern Chern, Yu-Ting Chen, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion. Taiwan J Obstet Gynecol 2011; 50:506-511.

Yi-Hui Lin, Chih-Ping Chen, Tze-Chien Chen, Chun-Sen Hsu, Szu-Yuan Chou, Shu-Chin Chien. Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction. Taiwan J Obstet Gynecol 2011; 50:528-530.

Chih-Ping Chen, Fang-Yu Hung, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Chen-Chi Lee, Yu-Ting Chen, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of mosaic trisomy 9. Taiwan J Obstet Gynecol 2011; 50:549-553.

Chih-Ping Chen, Yi-Ning Su, Chin-Yuan Hsu, Yu-Peng Liu, Schu-Rern Chern, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly. Taiwan J Obstet Gynecol 2011; 50:554-557.

Chih-Ping Chen, Yi-Yung Chen, Jun-Wei Su, Wayseen Wang. First trimester two-dimensional and three-dimensional ultrasound demonstration of craniofacial defects, abdominal wall defects and upper limb deficiency associated with limb-body wall complex. Taiwan J Obstet Gynecol 2011; 50:558-560.

Chih-Ping Chen, Chin-Yuan Hsu, Maw-Shuan Lee, Yu-Peng Liu, Fuu-Jen Tsai, Pei-Chen Wu, Schu-Rern Chern, Wayseen Wang. Magnetic resonance imaging demonstration of sirenomelia in one fetus of a dizygotic twin pregnancy conceived by intracytoplasmic sperm injection, in vitro fertilization and embryo transfer. Taiwan J Obstet Gynecol 2011; 50:561-563.

Cherry Yin-Yi Chang, Hui-Wen Chang, Chih-Mei Chen, Chia-Ying Lin, Chih-Ping Chen, Chih-Ho Lai, Wei-Yong Lin, Hsing-Ping Liu, Jim Jinn-Chyuan Sheu, Fuu-Jen Tsai. MUC4 gene polymorphisms associate with endometriosis development and endometriosis-related infertility. BMC Med. 2011; 9: 19.

Wei-De Lin, Shuan-Pei Lin, Chung-Hsing Wang, Yushin Tsai, Chih-Ping Chen, Fuu-Jen Tsai. RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia. Genet Mol Biol 2011; 34: 201–204.

Chia-Cheng Hung, Shin-Yu Lin, Chien-Nan Lee, Chih-Ping Chen, Shuan-Pei Lin, Mei-Chyn Chao, Shyh-Shin Chiou, Yi-Ning Su. Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene. BMC Med Genet. 2011; 12: 76.

Chia-Cheng Hung, Shin-Yu Lin, Shuan-Pei Lin, Chih-Ping Chen, Lang-Yao Chen, Chien-Nan Lee, Yi-Ning Su. Quantitative and qualitative analyses of the SNRPN gene using real-time PCR with melting curve analysis. J Mol Diagn 2011; 13: 609-613.

Yao-Yuan, Hsieh, Chi-Chen Chang, Yu-Kuo Wang, Kung-Hao Hsu, Chih-Ping Chen, Chin-Mu Hsu, Fuu-Jen Tsai. Insulin-like growth factors II exon 9 and E-cadherin-Pml I but not myeloperoxidase promoter-463, urokinase-ApaL I nor xeroderma pigmentosum polymorphisms are associated with higher susceptibility to leiomyoma. Anticancer Res 2010; 30: 2203-2208.

Chi-Yuan Chen, Hsiao-Hsuan Wu, Chih-Ping Chen, Schu-Rern Chern, Shiaw-Min Hwang, Shiu-Feng Huang, Wen-Hsin Lo, Guan-Yu Chen, Yu-Chen Hu. Biosafety assessment of human mesenchymal stem cells engineered by hybrid baculovirus vectors. Mol Pharm 2011; 8: 1505-1514.

Evangelyn Dominguez, Ting-Yu Chin, Chih-Ping Chen, Tzong-Yuan Wu. Management of moderate to severe Alzheimer's disease: Focus on memantine. Taiwan J Obstet Gynecol 2011; 50:415-423.

Shou-Jen Kuo, Gwo-Chin Ma, Shun-Ping Chang, Hsin-Hung Wu, Chih-Ping Chen, Tung-Ming Chang, Wen-Hsiang Lin, Sheng-Hai Wu, Mei-Hui Lee, Wuh-Liang Hwu, Ming Chen. Preimplantation and prenatal genetic diagnosis of aromatic L-amino acid decarboxylase deficiency with an amplification refractory mutation system-quantitative polymerase chain reaction. Taiwan J Obstet Gynecol 2011; 50:468-473.

Chih-Ping Chen, Shuan-Pei Lin, Dar-Shong Lin, Yu-Peng Liu, Lee James Hsu, Wayseen Wang. Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndrome. Genet Couns 2012; 23: 1-7.

Chih-Ping Chen. Prenatal diagnosis and genetic analysis of fetal akinesia deformation sequence and multiple pterygium syndrome associated with neuromuscular junction disorders: a review. Taiwan J Obstet Gynecol 2012; 51: 12-17.

Chih-Ping Chen, Yi-Hui Lin, Szu-Yuan Chou, Yi-Ning Su, Schu-Rern Chern, Yu-Ting Chen, Dai-Dyi Town, Wen-Lin Chen, Chen-Wen Pan, Wayseen Wang. Mosaic ring chromosome 21, monosomy 21 and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3. Taiwan J Obstet Gynecol 2012; 51: 71-76.

Chih-Ping Chen, Hsu-Kuang Huang, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Yu-Ting Chen, Wayseen Wang. Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR and aCGH analyses on uncultured amniocytes for rapid distinguishing true mosaicism from pseudomosaicism. Taiwan J Obstet Gynecol 2012; 51: 77-82.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Fuu-Jen Tsai, Pei-Chen Wu, Dai-Dyi Town, Li-Feng Chen, Meng-Shan Lee, Wayseen Wang. Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes. Taiwan J Obstet Gynecol 2012; 51: 93-99.

Chih-Ping Chen, Tung-Yao Chang, Tao-Yeuan Wang, Chen-Yu Chen, Fuu-Jen Tsai, Pei-Chen Wu, Schu-Rern Chern, Wayseen Wang. Short rib-polydactyly syndrome type II (Majewski): Prenatal diagnosis, perinatal imaging findings and molecular analysis of the NEK1 gene. Taiwan J Obstet Gynecol 2012; 51: 100-105.

Chih-Ping Chen, Yi-Ning Su, Chih-Long Chang, Yi-Yung Chen, Jun-Wei Su, Schu-Rern Chern, Wayseen Wang. Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification using uncultured amniocytes in pregnancy with major fetal structural abnormalities. Taiwan J Obstet Gynecol 2012; 51: 123-128.

Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Chin-Yuan Hsu, Yi-Yung Chen, Jun-Wei Su, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester. Taiwan J Obstet Gynecol 2012; 51: 129-133.

Chih-Ping Chen, Yi-Ning Su, Ming Chen, Fuu-Jen Tsai, Yi-Yung Chen, Gwo-Chin Ma, Shun-Ping Chang, Jun-Wei Su, Yu-Ting Chen, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism. Taiwan J Obstet Gynecol 2012; 51: 134-138.

Chih-Ping Chen, Jin-Chung Shih, Ming-Chao Huang, Yu-Peng Liu, Jun-Wei Su, Schu-Rern Chern, Wayseen Wang. Prenatal ultrasound demonstration of scoliosis, absence of one rib, a radial club hand, congenital heart defects and absent stomach in a fetus with VACTERL association. Taiwan J Obstet Gynecol 2012; 51: 139-142.

Chih-Ping Chen, Tung-Yao Chang, Chin-Yuan Hsu, Yu-Peng Liu, Fuu-Jen Tsai, Pei-Chen Wu, Wayseen Wang Wayseen Wang. Persistent cloaca presenting with a perineal cyst: prenatal ultrasound and magnetic resonance imaging findings. J Chin Med Assoc 2012; 75: 190-193.

Chih-Ping Chen, Jin-Chung Shih, Chen-Yu Chen, Yu-Peng Liu, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Prenatal Ultrasound and Magnetic Resonance Imaging Findings of Fetal Akinesia Deformation Sequence with Multiple Pterygium Syndrome J Med Ultrasound 2012; 20: 61-63.

Y-S Yang, Gwo-Chin Ma, Jin-Chung Shih, Chih-Ping Chen, C-H Chou, K-T Yeh, Shou-Jen Kuo, T-H Chen, Wuh-Liang Hwu, T-H Lee, Ming Chen. Experimental treatment of bilateral fetal chylothorax using in-utero pleurodesis. Ultrasound Obstet Gynecol 2012; 39: 56-62.

Yi-Jen Chen, Ying-Jay Liou, Chia-Ming Chang, Hsin-Yang Li, Chih-Yao Chen, Nae-Fang Twu, Ming-Shyen Yen, Yuh-Lih Chang, Chi-Hsien Peng, Shih-Hwa Chiou, Chih-Ping Chen, Kuan-Chong Chao. Reprogramming human endometrial fibroblast into induced pluripotent stem cells. Taiwan J Obstet Gynecol 2012; 51: 35-42.

Shun-Jen Tan, Chi-Huang Chen, Chih-Ping Chen, Chun-Wen Chen, Cheng-Yu Chen, Kwei-Shuai Hwang. Prenatal diagnosis of mosaic ring chromosome 15 with abnormal maternal serum Down syndrome screening and Dandy- Walker malformation. Taiwan J Obstet Gynecol 2012; 51: 109-111.

Cherry Yin-Yi Chang, Yi Chen, Wu-Chou Lin, Chih-Mei Chen, Chih-Ping Chen, Shan-Chih Lee, Jim Jinn-Chyuan Sheu and Fuu-Jen Tsai. MUC2 polymorphisms are associated with endometriosis development and infertility: a case-control study. BMC Med Genet 2012; 13: 15.

Yao-Yuan, Hsieh, Chi-Chen Chang, Shih-Yin Chen, Chih-Ping Chen, Wen-Hsin Lin, Fuu-Jen Tsai. XRCC1 399 Arg-related genotype and allele, but not XRCC1 His107Arg, XRCC1 Trp194Arg, KCNQ2, AT1R, and hOGG1 polymorphisms, are associated with higher susceptibility of endometriosis. Gynecol Endocrinol 2012; 28: 305-309.

Chen-Hsiang Yeang, Gwo-Chin Ma, Jin-Chung Shih, Yu-Shih Yang, Chih-Ping Chen, Shun-Ping Chang, Sheng-Hai Wu, Chin-San Liu, Shou-Jen Kuo, Hung-Chieh Chou, Wuh-Liang Hwu, Alan D. Cameron, Norman A. Ginsberg, Yi-Shing Lin, Ming Chen. Genome-wide gene expression analysis implicates the immune response and lymphangiogenesis in the pathogenesis of fetal chylothorax. PLoS One 2012 ;7: e34901.

Chassaing N, Sorrentino S, Davis EE, Martin-Coignard D, Iacovelli A, Paznekas W, Webb BD, Faye-Petersen O, Encha-Razavi F, Lequeux L, Vigouroux A, Yesilyurt A, Boyadjiev SA, Kayserili H, Loget P, Carles D, Sergi C, Puvabanditsin S, Chih-Ping Chen, Etchevers HC, Katsanis N, Mercer CL, Calvas P, Jabs EW. OTX2 mutations contribute to the otocephaly-dysgnathia complex. J Med Genet 2012; 49: 373-9.

Chih-Ping Chen, Shuan-Pei Lin, Ming-Ren Chen, Jun-Wei Su, Schu-Rern Chern, Yen-Jiun Chen, Meng-Shan Lee, Wayseen Wang. Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly. Genet Couns 2012; 23: 195-200.

Chih-Ping Chen, Hsien-Ming Lin, Cheung Leung, Shuan-Pei Lin, Yi-Ning Su, Jun-Wei Su, Yu-Ting Chen, Wayseen Wang. Partial monosomy 9p (9p22.2-->pter) and partial trisomy 18q (18q21.32-->qter) in a female infant with anorectal malformation. Genet Couns 2012; 23: 201-206.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Jun-Wei Su, Schu-Rern Chern, Dai-Dyi Town, Wayseen Wang. Pure distal 9p deletion in a female infant with cerebral palsy. Genet Couns 2012; 23: 215-221.

Chih-Ping Chen, Shuan-Pei Lin, Chyong-Hsin Hsu, Schu-Rern Chern, Jun-Wei Su, Yen-Jiun Chen, Chen-Wen Pan, Wayseen Wang. Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocation. Genet Couns 2012; 23: 223-229.

Chih-Ping Chen, Shuan-Pei Lin, Jun-Wei Su, Dai-Dyi Town, Wayseen Wang. A de novo supernumerary marker chromosome derived from chromosome 9p (9p13.1-->p23) associated with attention deficit and hyperactivity disorder. Genet Couns 2012; 23: 329-333.

Chih-Ping Chen, Shuan-Pei Lin, Jun-Wei Su, Meng-Shan Lee, Wayseen Wang. Phenotypic features associated with mosaic tetrasomy 9p in a 20-year-old female patient include autism spectrum disorder. Genet Couns 2012; 23: 335-338.

Chih-Ping Chen. Prenatal findings and genetic diagnosis of fetal overgrowth disorders: Simpson-Golabi-Behmel syndrome, Sotos syndrome and Beckwith-Wiedemann syndrome. Taiwan J Obstet Gynecol 2012; 51: 186-191.

Chih-Ping Chen, Ming Chen, Yi-Ning Su, Jian-Pei Huang, Gwo-Chin Ma, Shun-Ping Chang, Schu-Rern Chern, Yu-Ting Chen, Jun-Wei Su, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang. Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements. Taiwan J Obstet Gynecol 2012; 51: 245-252.

Chih-Ping Chen, Yi-Ning Su, Chih-Long Chang, Yi-Yung Chen, Jun-Wei Su, Schu-Rern Chern, Wayseen Wang. Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification using uncultured amniocytes in pregnancy with major fetal structural abnormalities. Taiwan J Obstet Gynecol 2012; 51: 123-128.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Ming-Huei Lin, Jun-Wei Su, Wayseen Wang. Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome. Taiwan J Obstet Gynecol 2012; 51: 271-275.

Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Chen-Yu Chen, Jun-Wei Su, Wayseen Wang. Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the asymptomatic father. Taiwan J Obstet Gynecol 2012; 51: 276-279.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Jian-Pei Huang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Uncomplicated vaginal delivery in two consecutive pregnancies carried to term in a woman with osteogenesis imperfecta type I and bisphosphonate treatment before conception. Taiwan J Obstet Gynecol 2012; 51: 305-307.

Chih-Ping Chen, Yi-Ning Su, Fang-Yu Hung, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II Taiwan J Obstet Gynecol 2012; 51: 308-311.

Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II. Taiwan J Obstet Gynecol 2012; 51: 312-314.

Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Ming-Chao Huang, Chun-Heng Pan, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Osteogenesis imperfecta type II: prenatal diagnosis and association with increased nuchal translucency and hypoechogenicity of the cranium. Taiwan J Obstet Gynecol 2012; 51: 315-318.

Chih-Ping Chen, You-Hsuan Chen, Schu-Rern Chern, Shing-Jyh Chang, Te-Lung Tsai, Sheng-Hsiang Li, Hsiu-Chuan Chou, Yi-Wen Lo, Ping-Chiang Lyu, Hong-Lin Chan. Placenta proteome analysis from Down syndrome pregnancies for biomarker discovery. Mol BioSyst 2012; 8: 2360-2372.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type III. Genet Couns 2012; 23: 359-365.

Chih-Ping Chen, Shuan-Pei Lin, Ming-Ren Chen, Yi-Ning Su, Schu-Rern Chern, Yu-Peng Liu, Jun-Wei Su, Meng-Shan Lee, Wayseen Wang. Partial monosomy 3p (3p26.2-->pter) and partial trisomy 5q (5q34-->qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay. Genet Couns 2012; 23: 405-413.

Chih-Ping Chen, Shuenn-Dyh Chang, Yi-Ning Su, Ming Chen, Schu-Rern Chern, Jun-Wei Su, Yu-Ting Chen, Wen-Lin Chen, Chen-Wen Pan, Meng-Shan Lee, Wayseen Wang. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase FISH, QF-PCR and aCGH on uncultured amniocytes in a pregnancy with fetal pyelectasis. Taiwan J Obstet Gynecol 2012; 51: 405-410.

Chih-Ping Chen, Ming Chen, Schu-Rern Chern, Peih-Shan Wu, Shun-Ping Chang, Dong-Jay Lee, Yu-Ting Chen, Li-Feng Chen, Jun-Wei Su, Alan Hwa-Ruey Hsieh, Alex Hwa-Jiun Hsieh, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2. Taiwan J Obstet Gynecol 2012; 51: 411-417.

Chih-Ping Chen, Schu-Rern Chern, Yi-Yung Chen, Pei-Chen Wu, Dai-Dyi Town, Wen-Lin Chen, Wayseen Wang. Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise. Taiwan J Obstet Gynecol 2012; 51: 430-434.

Chih-Ping Chen, Yi-Ning Su, Chen-Yu Chen, Jun-Wei Su, Schu-Rern Chern, Dai-Dyi Town, Wayseen Wang. Pure partial monosomy 3p (3p25.3→pter): prenatal diagnosis and array comparative genomic hybridization characterization. Taiwan J Obstet Gynecol 2012; 51: 435-439.

Chih-Ping Chen, Yi-Ning Su, Yi-Yung Chen, Schu-Rern Chern, Jun-Wei Su, Yu-Ting Chen, Dai-Dyi Town, Wayseen Wang. Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly. Taiwan J Obstet Gynecol 2012; 51: 471-474.

Chih-Ping Chen, Shuenn-Dyh Chang, Ho-Yen Chueh, Yi-Ning Su, Jun-Wei Su, Schu-Rern Chern, Yu-Ting Chen, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Li-Feng Chen, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang. Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes. Taiwan J Obstet Gynecol 2012; 51: 475-480.

Chih-Ping Chen, Yi-Ning Su, Shun-Long Weng, Fuu-Jen Tsai, Chen-Yu Chen, Yu-Peng Liu, Schu-Rern Chern, Wen-Lin Chen, Pei-Chen Wu, Wayseen Wang. Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester. Taiwan J Obstet Gynecol 2012; 51: 481-484.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Yu-Ting Chen, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation. Taiwan J Obstet Gynecol 2012; 51: 485-488.

Jian-Pei Huang, Chie-Pein Chen, Chih-Ping Chen, Kuo-Gon Wang, Kung-Liahng Wang. Term pregnancy with umbilical cord prolapse. Taiwan J Obstet Gynecol 2012; 51: 375-380.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Shuenn-Dyh Chang, Shu-Hang Ng, Yu-Peng Liu, Jun-Wei Su, Wayseen Wang. A de novo 4.4-Mb microdeletion in 2p24.3→p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome. Eur J Med Genet 2012; 55: 666-669.

Oliver B. Villaflores, Ying-Ju Chen, Chih-Ping Chen, Jui-Ming Yeh, Tzong-Yuan Wu. Curcuminoids and resveratrol as anti-Alzheimer agents. Taiwan J Obstet Gynecol 2012; 51: 515-525.

Oliver B. Villaflores, Ying-Ju Chen, Chih-Ping Chen, Jui-Ming Yeh, Tzong-Yuan Wu. Effects of curcumin and demethoxycurcumin on amyloid-β precursor and tau proteins through the internal ribosome entry sites: A potential therapeutic for Alzheimer’s disease. Taiwan J Obstet Gynecol 2012; 51: 554-564.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Yu-Ting Chen, Peih-Shan Wu, Jun-Wei Su, Chen-Wen Pan, Wayseen Wang. Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis. Taiwan J Obstet Gynecol 2012; 51: 603-611.

Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Yu-Ting Chen, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis of mosaic tetrasomy 18p. Taiwan J Obstet Gynecol 2012; 51: 625-629.

Chih-Ping Chen, Tsung-Hsien Su, Schu-Rern Chern, Jun-Wei Su, Chen-Chi Lee, Wayseen Wang. Alobar holoprosencephaly, cebocephaly and micropenis in a Klinefelter fetus of a diabetic mother. Taiwan J Obstet Gynecol 2012; 51: 630-634.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. First-trimester prenatal diagnosis of Ellis-van Creveld syndrome. Taiwan J Obstet Gynecol 2012; 51: 643-648.

Chih-Ping Chen, Shuenn-Dyh Chang, Yu-Ting Chen, Jun-Wei Su, Dai-Dyi Town, Wayseen Wang. Mosaic isochromosome 20q detected at amniocentesis: a likely cell culture artifact. Taiwan J Obstet Gynecol 2012; 51: 663-665.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Yu-Ting Chen, Jun-Wei Su, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis of trisomy 8 mosaicism. Taiwan J Obstet Gynecol 2012; 51: 666-668.

Chih-Ping Chen, Pei-Chen Wu, Fuu-Jen Tsai, Li-Feng Chen, Wayseen Wang. Detection of mosaic balanced homologous acrocentric rearrangement rea(21q21q) in a woman with repeated pregnancy losses. Taiwan J Obstet Gynecol 2012; 51: 669-671.

Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis of an interstitial deletion of 10q (10q11.21®q21.1): array comparative genomic hybridization characterization and literature review. Taiwan J Obstet Gynecol 2012; 51: 672-676.

Chi-Fung Chen, Chih-Ping Chen, Chung-Der Hsiao. Zebrafish research in Taiwan. Hereditas 2012; 34: 1089-1096.

Longoni M, Lage K, Russell MK, Loscertales M, Abdul-Rahman OA, Baynam G, Bleyl SB, Brady PD, Breckpot J, Chih-Ping Chen, Devriendt K, Gillessen-Kaesbach G, Grix AW, Rope AF, Shimokawa O, Strauss B, Wieczorek D, Zackai EH, Coletti CM, Maalouf FI, Noonan KM, Park JH, Tracy AA, Lee C, Donahoe PK, Pober BR. Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks. Am J Med Genet 2012; 158A: 3148-3158.

Chih-Ping Chen, Tzu-Chia Lai, Schu-Rern Chern, Sheng-Hsiang Li, Hsiu-Chuan Chou, Yi-Wen Chen, Szu-Ting Lin, Ying-Chieh Lu, Chieh-Lin Wu, Ji-Min Li, Hong-Lin Chan. Proteome differences between male and female fetal cells in amniotic fluid. OMICS 2013; 17: 16-26.

Chih-Ping Chen, Ming Chen, Gwo-Chin Ma, Yi-Ning Su, Tsang-Ming Ko, Yi-Hui Lin, Wayseen Wang. Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosome. J Chin Med Assoc 2013; 76: 53-56.

Ming-Chao Huang, Ching-Hung Hsieh, Tsung-Hsien Su, Chih-Ping Chen, Tze-Yi Yang, Kung-Liahng Wang, Maw-Sheng Lee. Safety and efficacy of unidirectional barbed suture in mini-laparotomy myomectomy. Taiwan J Obstet Gynecol 2013; 52: 53-56.

Chih-Ping Chen, Yi-Ning Su, Jun-Wei Su, Schu-Rern Chern, Yu-Ting Chen, Li-Feng Chen, Wayseen Wang. Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis. Taiwan J Obstet Gynecol 2013; 52: 97-105.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism. Taiwan J Obstet Gynecol 2013; 52: 106-109.

Chih-Ping Chen, Yi-Ning Su, Shuan-Pei Lin, Schu-Rern Chern, Jun-Wei Su, Yu-Ting Chen, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry. Taiwan J Obstet Gynecol 2013; 52: 120-124.

Chih-Ping Chen, Kwui-Shuai Hwang, Her-Young Su, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Yu-Ting Chen, Jun-Wei Su, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry. Taiwan J Obstet Gynecol 2013; 52: 125-128.

Chih-Ping Chen, Shuenn-Dyh Chang, Ho-Yen Chueh, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Yu-Ting Chen, Li-Feng Chen, Meng-Shan Lee, Wayseen Wang. Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20. Taiwan J Obstet Gynecol 2013; 52: 145-146.

Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Jun-Wei Su, Yu-Ting Chen, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21). Taiwan J Obstet Gynecol 2013; 52: 147-151.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome. Taiwan J Obstet Gynecol 2013; 52: 152-153.

Chih-Ping Chen, Chin-Yuan Hsu, Yi-Ning Su, Tao-Yeuan Wang, Yi-Yung Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma and intrauterine growth restriction. Taiwan J Obstet Gynecol 2013; 52: 154-156.

Chih-Ping Chen, Jun-Wei Su, Chia-Heng Lee, Wayseen Wang. Incidental detection of thoracoomphalopagus at amniocentesis in a twin pregnancy. J Med Ultrasound 2013; 21: 46-48.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wayseen Wang. A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 gene. Genet Couns 2013; 24: 243-246.

Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Chen-Yu Chen, Jun-Wei Su, Wayseen Wang. Rapid detection of de novo P253R mutation in FGFR2 using uncultured amniocytes in a pregnancy affected by polyhydramnios, Blake’s pouch cyst and Apert syndrome. Taiwan J Obstet Gynecol 2013; 52: 273-277.

Chih-Ping Chen, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization. Taiwan J Obstet Gynecol 2013; 52: 154-156.

Chih-Ping Chen, Ming-Chao Huang, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wayseen Wang. Discordant anencephaly and Cantrell syndrome in monozygotic twins conceived by ICSI and IVF-ET. Taiwan J Obstet Gynecol 2013; 52: 297-299.

Chih-Ping Chen, Fang-Yu Hung, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wayseen Wang. Application of interphase FISH on uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a single colony. Taiwan J Obstet Gynecol 2013; 52: 300-302.

Chih-Ping Chen, Chen-Ju Lin, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wayseen Wang. Maternal transmission of interstitial microdeletion of 5q13.2 detected during prenatal diagnosis of coarctation of the aorta. Taiwan J Obstet Gynecol 2013; 52: 303-305.

Pen-Hwa Su, Chih-Ping Chen, Yi-Ning Su, Su-Jen Chen, L-L Lin, J-Y Chen. Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13. Genet Mol Res 2013; 12: 1311-1317.

Chih-Ping Chen, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly and facial dysmorphism. Taiwan J Obstet Gynecol 2013; 52: 395-400.

Chih-Ping Chen, Chung-Hu Fu, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Chi Lee, Meng-Shan Lee, Wayseen Wang. De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1→pter) and 14q (14q32.31→qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction and single umbilical artery: prenatal diagnosis and molecular cytogenetic characterization. Taiwan J Obstet Gynecol 2013; 52: 401-406.

Chih-Ping Chen, Tung-Yao Chang, Wan-Yuo Guo, Yi-Ning Su, Yi-Yung Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of maternal epilepsy. Taiwan J Obstet Gynecol 2013; 52: 415-419.

Chih-Ping Chen, Tung-Yao Chang, Ming-Huei Lin, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs and thanatophoric dysplasia type II. Taiwan J Obstet Gynecol 2013; 52: 420-425.

Chih-Ping Chen, Kuo-Gon Wang, Tsang-Ming Ko, Schu-Rern Chern, Jun-Wei Su, Dai-Dyi Town, Wayseen Wang. Mosaic trisomy 14 at amniocentesis: prenatal diagnosis and literature review. Taiwan J Obstet Gynecol 2013; 52: 446-449.

Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang. Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis. Taiwan J Obstet Gynecol 2013; 52: 450-453.

Chih-Ping Chen, Shing-Jyh Chang, Jun-Wei Su, Yu-Ting Chen, Wayseen Wang. Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth. Taiwan J Obstet Gynecol 2013; 52: 454-456.

Sheng-Wen Steven Shaw, Chih-Ping Chen, Po-Jen Cheng. From Down syndrome screening to noninvasive prenatal testing: 20 years' experience in Taiwan. Taiwan J Obstet Gynecol 2013; 52: 470-474.

Chih-Ping Chen, Shuenn-Dyh Chang, Tzu-Hao Wang, Liang-Kai Wang, Jeng-Daw Tsai, Yu-Peng Liu, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Wayseen Wang. Detection of recurrent transmission of 17q12 microdeletion by aCGH in a fetus with prenatally diagnosed hydronephrosis, hydroureter and multicystic kidney, and variable clinical spectrum in the family. Taiwan J Obstet Gynecol 2013; 52: 551-557.

Chih-Ping Chen, Chen-Yu Chen, Jun-Wei Su, Wayseen Wang. Female pseudohermaphroditism in a prenatally diagnosed cloacal malformation with hydronephrosis, dilated bladder, hydrometrocolpos and oligohydramnios. Taiwan J Obstet Gynecol 2013; 52: 571-574.

Chih-Ping Chen, Tung-Yao Chang, Yi-Yung Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer. Taiwan J Obstet Gynecol 2013; 52: 575-579.

Chih-Ping Chen, Yi-Ning Su, Tzu-Hung Lin, Tung-Yao Chang, Jun-Wei Su, Wayseen Wang. Detection of de novo Y278C mutation in FGFR3 in a pregnancy affected with fetal severe hypochondroplasia: prenatal diagnosis and literature review. Taiwan J Obstet Gynecol 2013; 52: 580-585.

Pi-Lin Sung, Eong-Eong Cheng, Yann-Jang Chen, Schu-Rern Chern, Chung-Yu Shih, Chia-Ming Chang, Peng-Hui Wang, Ming-Shyen Yen, Chi-Ying F. Huang, Chih-Ping Chen. Prenatal diagnosis of de novo monosomy 7q33-qter associated with hydrops fetalis, semilobar holoprosencephaly, and premaxillary dysgenesis. Taiwan J Obstet Gynecol 2013; 52: 602-606.

Chih-Ping Chen, Hsu-Kuang Huang, Yu-Peng Liu, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis. Taiwan J Obstet Gynecol 2013; 52: 607-610.

Chih-Ping Chen, Yuh-Ming Hwu, Chen-Yu Chen, Yi-Ning Su, Tzu-Hung Lin, Yu-Ling Kuo, Schu-Rern Chern, Wayseen Wang. Concordant myelomeningocele in dizygotic twins conceived by intracytoplasmic sperm injection, in vitro fertilization and embryo transfer. Taiwan J Obstet Gynecol 2013; 52: 611-612.

Chih-Ping Chen, Hsu-Kuang Huang, Yu-Peng Liu, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang. First-trimester sonographic demonstration of digynic triploidy. Taiwan J Obstet Gynecol 2013; 52: 613-615.

Chih-Ping Chen, Yao-Lung Chang, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints. Gene 2013; 516: 132-137.

Chih-Ping Chen, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold. Gene 2013; 516: 138-142.

Chih-Ping Chen, Chen-Ju Lin, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Jun-Wei Su, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization. Gene 2013; 519: 164-168.

Chih-Ping Chen, Shing-Jyh Chang, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Jun-Wei Su, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1). Gene 2013; 521: 311-315.

Chih-Ping Chen, Po-Jen Cheng, Shuenn-Dyh Chang, Yi-Xuan Lee, Jin-Chung Shih, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Adam Hwa-Ming Hsieh, Teresa Hsiao-Tien Chen, Li-Feng Chen, Wayseen Wang. Ring chromosome 21 presenting with sacrococcygeal teratoma: prenatal diagnosis, molecular cytogenetic characterization and literature review. Gene 2013; 522: 111-116.

Chih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Jun-Wei Su, Chen-Chi Lee, Wayseen Wang. 6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia, psychomotor developmental delay and poor wound healing. Gene 2013; 523: 99-102.

Chih-Ping Chen, Ming-Chao Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Jun-Wei Su, Wayseen Wang. Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: prenatal diagnosis and aCGH characterization using uncultured amniocytes. Gene 2013; 524: 407-411.

Chih-Ping Chen, Tsang-Ming Ko, Yi-Yung Chen, Jun-Wei Su, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome. Gene 2013; 527: 384-388.

Chih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Wen-Lin Chen, Wayseen Wang. Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review. Gene 2013; 527: 405-409.

Chih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Wen Pan, Wayseen Wang. Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes. Gene 2013; 527: 636-641.

Chih-Ping Chen, Chin-Han Tsai, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Chi Lee, Yu-Ting Chen, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13. Gene 2013; 529: 163-168.

Chih-Ping Chen, Ming Chen, Yi-Ning Su, Jian-Pei Huang, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Shun-Ping Chang, Yu-Ting Chen, Chen-Chi Lee, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang. Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review. Gene 2013; 529: 169-175.

Chih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Chen-Chi Lee, Wayseen Wang. An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy. Gene 2013; 529: 176-180.

Chih-Ping Chen, Meng-Ju Lee, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2→p14). Gene 2013; 529: 351-356.

Chih-Ping Chen, Yi-Ning Su, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review. Genomics 2013; 102: 265-269

Chih-Ping Chen, Ming-Chao Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Jun-Wei Su, Wayseen Wang. Prenatal diagnosis of de novo cryptic microdeletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect. Gene 2013; 531: 496-501.

Chih-Ping Chen, Chen-Ju Lin, Yi-Yung Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Li-Feng Chen, Dai-Dyi Town, Chen-Wen Pan, Wayseen Wang. 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization. Gene 2013; 532: 80-86.

Chih-Ping Chen, Tung-Yao Chang, Wan-Yuo Guo, Pei-Chen Wu, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Li-Feng Chen, Wayseen Wang. Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review. Gene 2013; 532: 152-159.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Yu-Ling Kuo, Peih-Shan Wu, Yu-Ting Chen, Meng-Shan Lee, Wayseen Wang. Array CGH characterization of an unbalanced X-autosome translocation associated with Xq27.2-qter deletion, 11q24.3-qter duplication and Xq22.3-q27.1 duplication in a girl with primary amenorrhea and mental retardation. Gene 2014; 535: 88-92.

Chih-Ping Chen, Ming Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shun-Ping Chang, Yu-Ling Kuo, Wen-Lin Chen, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry. Gene 2014; 536: 425-429.

Kuan-Hao Tsui, Wen-Ling Lee, Kok-Min Seow, Lin-Wei Yang, Shih-Yi Wang, Peng-Hui Wang, Chi-Lun Chang, Ming-Shyen Yen, Jiin-Tsuey Cheng, Chih-Ping Chen. Effect of gonadotropin-releasing hormone agonist on ES-2 ovarian cancer cells. Taiwan J Obstet Gynecol 2014; 53: 35-42.

Chen-Ju Lin, Chih-Ping Chen, Shu-Chin Chien, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, L i-Feng Chen, Meng-Shan Lee, Chen-Wen Pan, Ku-Chien Lin, Tze-Tien Yeh. Chromosomal deletions detected at amniocentesis. Taiwan J Obstet Gynecol 2014; 53: 62-37.

Chih-Ping Chen, Yi-Ning Su, Ming-Huei Lin, Tao-Yeuan Wang, Schu-Rern Chern, Yu-Ling Kuo, Yu-Ting Chen, Wayseen Wang. Detection of altered methylation status at 11p15 and 7q32 in placental mesenchymal dysplasia. Taiwan J Obstet Gynecol 2014; 53: 68-73.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Chi Lee, Wayseen Wang. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation. Taiwan J Obstet Gynecol 2014; 53: 74-78.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Yu-Ling Kuo, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang. Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization and literature review. Taiwan J Obstet Gynecol 2014; 53: 79-85.

Chih-Ping Chen, Yi-Ning Su, Shee-Uan Chen, Tung-Yao Chang, Pei-Chen Wu, Schu-Rern Chern, Peih-Shan Wu, Yu-Ling Kuo, Wayseen Wang. Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET. Taiwan J Obstet Gynecol 2014; 53: 90-94.

Ling-Chao Chen, Chih-Yao Chen, Huann-Cheng Horng, Ming-Shyen Yen, Peng-Hui Wang, Chih-Ping Chen, Wen-Hsun Chang. Sex ratio at a tertiary medical center in northern Taiwan – An analysis of amniocentesis. Taiwan J Obstet Gynecol 2014; 53: 118-119.

Chih-Ping Chen, Pu-Tsui Wang, Shuan-Pei Lin, Schu-Rern Chern, Yu-Ting Chen, Peih-Shan Wu, Yu-Ling Kuo, Wen-Lin Chen, Wayseen Wang. Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes. Taiwan J Obstet Gynecol 2014; 53: 120-122.

Chih-Ping Chen, Ming-Huei Lin, Schu-Rern Chern, Yu-Ting Chen, Peih-Shan Wu, Yu-Ling Kuo, Meng-Shan Lee, Wayseen Wang. Directly transmitted 4.5-Mb triplication of 4q12-q13.1: prenatal diagnosis and molecular cytogenetic characterization. Taiwan J Obstet Gynecol 2014; 53: 123-125.

Chih-Ping Chen, Chen-Ju Lin, Tsang-Ming Ko, Schu-Rern Chern, Yu-Ting Chen, Peih-Shan Wu, Yu-Ling Kuo, Meng-Shan Lee, Wayseen Wang. Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p. Taiwan J Obstet Gynecol 2014; 53: 126-128.

Chih-Ping Chen, Ming Chen, Yi-Ning Su, Schu-Rern Chern, Peih-Shan Wu, Shun-Ping Chang, Yu-Ling Kuo, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15. Taiwan J Obstet Gynecol 2014; 53: 129-132.

Yu-Ling Kuo, Chih-Ping Chen, Liang-Kai Wang, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Shu-Yuan Chan. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects. Taiwan J Obstet Gynecol 2014; 53: 248-251.

Chih-Ping Chen, Cheng-Ran Peng, Schu-Rern Chern, Yu-Ling Kuo, Peih-Shan Wu, Dai-Dyi Town, Chen-Wen Pan, Chien-Wen Yang, Wayseen Wang. Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome. Taiwan J Obstet Gynecol 2014; 53: 566-571.

Chih-Ping Chen, Tsang-Ming Ko, Chen-Yu Chen, Tao-Yeuan Wang, Schu-Rern Chern, Yu-Ling Kuo, Wayseen Wang. First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination. Taiwan J Obstet Gynecol 2014; 53: 572-578.

Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Yu-Peng Liu, Yu-Ling Kuo, Peih-Shan Wu, Dai-Dyi Town, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome. Taiwan J Obstet Gynecol 2014; 53: 583-587.

Wen-Chien Hou, Chih-Ping Chen, Kwei-Shuai Hwang, Ying-Chieh Chen, Yu-Ju Lai, Chau-Yang Tien, Her-Young Su. Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in a fetus with major congenital anomalies. Taiwan J Obstet Gynecol 2014; 53: 602-605.

Shwu-Meei Wang, Ya-Ju Hsieh, Kuo-Ming Chang, Hsiang-Ling Tsai, Chih-Ping Chen. Schimmelpenning syndrome: a case report and literature review. Pediatr Neonatol 2014; 55: 487-490.

Chih-Ping Chen, Jun-Wei Su, Schu-Rern Chern, Yu-Ling Kuo, Peih-Shan Wu, Meng-Shan Lee, Chien-Wen Yang, Wayseen Wang. Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis Taiwan J Obstet Gynecol 2015; 54: 58-61.

Chih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, Yu-Peng Liu, Cheng-Ran Peng, Yu-Ling Kuo, Peih-Shan Wu, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia. Taiwan J Obstet Gynecol 2015; 54: 66-70.

Chih-Ping Chen, Tsang-Ming Ko, Ming-Chao Huang, Schu-Rern Chern, Tan-Wei Lin, Tung-Yao Chang, Yu-Ling Kuo, Wen-Lin Chen, Wayseen Wang. Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma. Taiwan J Obstet Gynecol 2015; 54: 78-80.

Ming-Chou Chiang, Jen-Fu Hsu, Chuen Hsueh, Hsun-Chin Chao, Tzu-Hao Wang, Chih-Ping Chen, Ming-Wei Lai. Bowel "dissection" in microvillus inclusion disease. Pediatr Neonatol 2015; 56: 129-131.

Peng-Hui Wang, Chih-Ping Chen. Noninvasive prenatal testing for fetal trisomy in mixed risk factors pregnancy population. Taiwan J Obstet Gynecol 2015; 54: 109-110.

Peng-Hui Wang, Chih-Ping Chen. Readers' comment is important for the journal. Taiwan J Obstet Gynecol 2015; 54:111.

Cheng-Ran Peng, Chih-Ping Chen, Kuo-Gon Wang, Liang-Kai Wang, Chen-Yu Chen, Yi-Yung Chen. The reliability of transabdominal cervical length measurement in a low-risk obstetric population: Comparison with transvaginal measurement. Taiwan J Obstet Gynecol 2015; 54: 167-171.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Yu-Ling Kuo, Yen-Ni Chen, Chen-Wen Pan, Wayseen Wang. First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism. Taiwan J Obstet Gynecol 2015; 54: 194-195.

Peng-Hui Wang, Chih-Ping Chen. Outstanding research paper awards of the 2014 Taiwanese Journal of Obstetrics and Gynecology. Taiwan J Obstet Gynecol 2015; 54: 215-216.

Chih-Ping Chen, Ming-Chao Huang, Schu-Rern Chern, Yu-Ling Kuo, Yen-Ni Chen, Peih-Shan Wu, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang. Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature. Taiwan J Obstet Gynecol 2015; 54: 297-302.

Yu-Jen Chang, Hong-Lin Su, Lee-Feng Hsu, Po-Jui Huang, Tzu-Hao Wang, Fu-Chou Cheng, Li-Wen Hsu, Ming-Song Tsai, Chih-Ping Chen, Yao-Lung Chang, An-Shine Chao, Shiaw-Min Hwang. Isolation of human neural stem cells from the amniotic fluid with diagnosed neural tube defects. Stem Cells Dev 2015; 24: 1740-1750.

Peng-Hui Wang, Chang-Ching Yeh, Yi-Jen Chen, Chih-Ping Chen. Maternal serum markers and preeclampsia. Taiwan J Obstet Gynecol 2015; 54: 339-340.

Wen-Ling Lee, Chih-Ping Chen, Peng-Hui Wang. Maternal serum markers and preeclampsia. Taiwan J Obstet Gynecol 2015; 54: 341-342.

Chih-Ping Chen, Schu-Rern Chern, Yen-Ni Chen, Peih-Shan Wu, Chien-Wen Yang, Li-Feng Chen, Wayseen Wang. Mosaic trisomy 15 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review. Taiwan J Obstet Gynecol 2015; 54: 426-431.

Chih-Ping Chen, Shuan-Pei Lin, Hui-Bo Li, Yen-Ni Chen, Wayseen Wang. Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening result. Taiwan J Obstet Gynecol 2015; 54: 450-451.

Sheng-Yuan Su, Ho-Yen Chueh, Ching-Pei Li, Yao-Lung Chang, Shuenn-Dyh Chang, Chih-Ping Chen. Interphase fluorescence in situ hybridization assisting in prenatal counseling for amniocentesis karyotyping-detected fetal mosaicism. Taiwan J Obstet Gynecol 2015; 54: 588-591.

Chih-Ping Chen, Ming-Huei Lin, Yi-Yung Chen, Schu-Rern Chern, Yen-Ni Chen, Peih-Shan Wu, Chen-Wen Pan, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome and Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1. Taiwan J Obstet Gynecol 2015; 54: 592-596.

Peng-Hui Wang, Chih-Ping Chen. Authors' responsibility is critical for journal. Taiwan J Obstet Gynecol 2015; 54: 633-634.

Chih-Ping Chen, Cheng-Ran Peng, Tung-Yao Chang, Wan-Yuo Guo, Yen-Ni Chen, Peih-Shan Wu, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly. Taiwan J Obstet Gynecol 2015; 54: 797-798.

Yen-Ni Chen, Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Pei-Chen Wu, Tung-Yao Chang, Peih-Shan Wu, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion. Taiwan J Obstet Gynecol 2016; 55: 117-120.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot. Taiwan J Obstet Gynecol 2016; 55: 270-274.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes. Taiwan J Obstet Gynecol 2016; 55: 285-287.

Chih-Ping Chen, Fang-Yu Hung, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3­→pter) and partial trisomy 16q (16q23.1→qter). Taiwan J Obstet Gynecol 2016; 55: 288-292.

Chih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome. Taiwan J Obstet Gynecol 2016; 55: 303-304.

Chih-Ping Chen, Tsang-Ming Ko, Wen-Chu Huang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Chen-Wen Pan, Chien-Wen Yang, Wayseen Wang. Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction. Taiwan J Obstet Gynecol 2016; 55: 415-418.

Chih-Ping Chen, Sheng Chiang, Kung-Liahng Wang, Fu-Nan Cho, Ming Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Shun-Ping Chang, Weu-Lin Chen, Wayseen Wang. Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay and speech delay. Taiwan J Obstet Gynecol 2016; 55: 419-422.

Chih-Ping Chen, Tung-Yao Chang, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wen-Lin Chen, Wayseen Wang. 22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae and congenital heart defects on prenatal ultrasound. Taiwan J Obstet Gynecol 2016; 55: 455-456.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Kevin Ko, Yen-Ni Chen, Shin-Wen Chen, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development and ventriculomegaly. Taiwan J Obstet Gynecol 2016; 55: 591-595.

Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication. Taiwan J Obstet Gynecol 2016; 55: 596-601.

Chih-Ping Chen, Shing-Jyh Chang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Chen-Wen Pan, Wayseen Wang. Rapid diagnosis of pseudomosaicism in a case of level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis. Taiwan J Obstet Gynecol 2016; 55: 602-603.

Hsiang-Yu Lin, Chih-Kuang Chuang, Ru-Yi Tu, Yi-Ya Fang, Yi-Ning Su, Chih-Ping Chen, Chia-Ying Chang, Hsi-Che Liu, Tzu-Hung Chu, Dau-Ming Niu, Shuan-Pei Lin. Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith-Wiedemann syndrome. Mol Genet Metab 2016; 119: 8-13.

Yen-Ni Chen, Chih-Ping Chen, Chen-Ju Lin, Shin-Wen Chen. Prenatal ultrasound findings of pregnancy associated with Zika virus infection. J Med Ultrasound 2016; 24: 89-92.

Peng-Hui Wang, Chih-Ping Chen. Outstanding research paper awards of the 2015 Taiwanese Journal of Obstetrics and Gynecolog. Taiwan J Obstet Gynecol 2016; 55: 623-624.

Peng-Hui Wang, Ming-Shyen Yen, Kuan-Chong Chao, Chih-Ping Chen. Outstanding female cancer research paper awards of the 2015 Taiwan Association of Obstetrics and Gynecology and Hsu Chien-Tien Cancer Foundation. Taiwan J Obstet Gynecol 2016; 55: 757-759.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Dai-Dyi Town, Meng-Shan Lee, Chien-Wen Yang, Wayseen Wang. Molecular cytogenetic characterization of Xp22.32®pter deletion and Xq26.3®qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq)inv(X)(p22.3q26.3), a hypoplastic left heart, short stature and maternal X chromosome pericentric inversion. Taiwan J Obstet Gynecol 2016; 55: 705-711.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Yen-Ni Chen, Shin-Wen Chen, Peih-Shan Wu, Dai-Dyi Town, Chen-Wen Pan, Chien-Wen Yang, Wayseen Wang. Mosaic trisomy 17 at amniocentesis: prenatal diagnosis, molecular genetic analysis, and literature review. Taiwan J Obstet Gynecol 2016; 55: 712-717.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Dai-Dyi Town, Chien-Wen Yang, Wayseen Wang. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome. Taiwan J Obstet Gynecol 2016; 55: 728-732.

Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Kevin Ko, Chen-Chi Lee, Dai-Dyi Town, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentirc inversion. Taiwan J Obstet Gynecol 2016; 55: 733-737.

Chih-Ping Chen, Chen-Yu Chen, Tung-Yao Chang, Hsiu-Yu Yang, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang. Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome. Taiwan J Obstet Gynecol 2016; 55: 745-747.

Chih-Ping Chen, Shuan-Pei Lin, Yi-Hui Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Wen-Lin Chen, Wayseen Wang. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities. Taiwan J Obstet Gynecol 2016; 55: 852-855.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Meng-Shan Lee, Wayseen Wang. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder and intellectual disability. Taiwan J Obstet Gynecol 2016; 55: 856-860.

Chih-Ping Chen, Chung-Hu Fu, Yi-Hui Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang. Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality. Taiwan J Obstet Gynecol 2016; 55: 871-873.

Chih-Ping Chen, Schu-Rern Chern, Nan-Chang Chiu, Yu-Peng Liu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang. Detection of a novel c.7106­_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling. Taiwan J Obstet Gynecol 2016; 55: 897-899.

Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome. Taiwan J Obstet Gynecol 2016; 55: 900-901.

Chih-Ping Chen, Fang-Yu Hung, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Meng-Shan Lee, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome. Taiwan J Obstet Gynecol 2016; 55: 902-903.

Shin-Wen Chen, Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Pei-Chen Wu, Yen-Ni Chen, Chen-Ju Lin, Wen-Ling Chen, Wayseen Wang. Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3. Taiwan J Obstet Gynecol 2017; 56: 87-92.

Chih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang. Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1 and TUBGCP5 associated with phenotypic variability in developmental, speech and motor delay. Taiwan J Obstet Gynecol 2017; 56: 93-97.

Chih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang. Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6 and BUB1 associated with autism spectrum disorder, intellectual disability and liver disorder. Taiwan J Obstet Gynecol 2017; 56: 98-101.

Chih-Ping Chen, Liang-Kai Wang, Pei-Chen Wu, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Chien-Wen Yang, Wayseen Wang. Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound. Taiwan J Obstet Gynecol 2017; 56: 102-105.

Chih-Ping Chen, Schu-Rern Chern, Yen-Ni Chen, Shin-Wen Chen, Peih-Shan Wu, Chien-Wen Yang, Chen-Chi Lee, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality. Taiwan J Obstet Gynecol 2017; 56: 217-223.

Chih-Ping Chen, Kuo-Gon Wang, Hsu-Kuang Huang, Cheng-Ran Peng, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Wayseen Wang. Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis. Taiwan J Obstet Gynecol 2017; 56: 230-233.

Chih-Ping Chen, Ming Chen, Shun-Ping Chang, Fang-Yu Hung, Meng-Ju Lee, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Dai-Dyi Town, Meng-Shan Lee, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2. Taiwan J Obstet Gynecol 2017; 56: 234-237.

Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Wen Pan, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome. Taiwan J Obstet Gynecol 2017; 56: 238-242.

Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Dai-Dyi Town, Meng-Shan Lee, Wayseen Wang. Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome. Taiwan J Obstet Gynecol 2017; 56: 264-267.

Chih-Ping Chen, Fang-Yu Hung, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome. Taiwan J Obstet Gynecol 2017; 56: 268-269.

Chih-Ping Chen, Hoi-Kin Yip, Liang-Kai Wang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Wayseen Wang. Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1. Taiwan J Obstet Gynecol 2017; 56: 385-389.

Chih-Ping Chen, Chang-Sheng Yin, Liang-Kai Wang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Wen-Lin Chen, Wayseen Wang. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p(20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome. Taiwan J Obstet Gynecol 2017; 56: 390-393.

Chih-Ping Chen, Ming Chen, Pu-Tsui Wang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Shun-Ping Chang, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11. Taiwan J Obstet Gynecol 2017; 56: 394-397.

Chih-Ping Chen, Chen-Ju Lin, Yen-Ni Chen, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Li-Feng Chen, Wayseen Wang. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency. Taiwan J Obstet Gynecol 2017; 56: 398-401.

Chih-Ping Chen, Ming Chen, Yuh-Ming Hwu, Shun-Ping Chang, Shin-Wen Chen, Shih-Ting Lai, Chen-Chi Lee, Wayseen Wang. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions. Taiwan J Obstet Gynecol 2017; 56: 410-411.

Chih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Wayseen Wang. Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia. Taiwan J Obstet Gynecol 2017; 56: 412-414.

Peng-Hui Wang, Chih-Ping Chen. Outstanding research paper awards of the 2016 Taiwanese Journal of Obstetrics and Gynecolog. Taiwan J Obstet Gynecol 2017; 56: 423-424.

Pei-Shan Tsai, Chih-Ping Chen, Dao Chen Lin, Yu-Peng Liu. Prenatal diagnosis of congenital lobar fluid overload. Taiwan J Obstet Gynecol 2016; 56: 425-431.

Chih-Ping Chen, Ming Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Shun-Ping Chang, Chien-Wen Yang, Chen-Wen Pan, Wayseen Wang. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9. Taiwan J Obstet Gynecol 2017; 56: 527-533.

Chih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Chien-Wen Yang, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16. Taiwan J Obstet Gynecol 2017; 56: 545-549.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Chen-Chi Lee, Chien-Wen Yang, Wayseen Wang. Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect. Taiwan J Obstet Gynecol 2017; 56: 550-553.

Chih-Ping Chen, Ming Chen, Chia-Hsun Wu, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Shun-Ping Chang, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review. Taiwan J Obstet Gynecol 2017; 56: 554-557.

Chih-Ping Chen, Ming Chen, Schu-Rern Chern, Shun-Ping Chang, Shin-Wen Chen, Shih-Ting Lai, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21. Taiwan J Obstet Gynecol 2017; 56: 566-568.

Chih-Ping Chen, Jian-Pei Huang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Chen-Chi Lee, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2017; 56: 569-570.

Peng-Hui Wang, Chih-Ping Chen, Tsung-Cheng Kuo. Outstanding female cancer research paper awards of the 2016 Taiwan Association of Obstetrics and Gynecology and Hsu Chien-Tien Cancer Foundation. Taiwan J Obstet Gynecol 2017; 56: 581-582.

Jhe-Jhih Lin, Ting-Yu Chin, Chih-Ping Chen, Hong-Lin Chan, Tzong-Yuan Wu. Zika virus: An emerging challenge for obstetrics and gynecology. Taiwan J Obstet Gynecol 2017; 56: 585-592.

Shih-Ting Lai, Chih-Ping Chen, Chen-Ju Lin, Yen-Ni Chen, Shin-Wen Chen. An intrauterine gestational sac surrounded by thin myometrium at fundus. J Med Ultrasound 2017; 25: 255-257.

Chih-Ping Chen, Chris Tsai, Ming-Huei Lin, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Wen-Lin Chen, Chen-Wen Pan, Wayseen Wang. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism. Taiwan J Obstet Gynecol 2017; 56: 691-693.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones. Taiwan J Obstet Gynecol 2017; 56: 821-826.

Chih-Ping Chen, Tsang-Ming Ko, Yi-Yung Chen, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2017; 56: 836-839.

Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome. Taiwan J Obstet Gynecol 2017; 56: 840-842.

Chih-Ping Chen, Tung-Yao Chang, Fang-Yu Hung, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound. Taiwan J Obstet Gynecol 2017; 56: 843-846.

Chih-Ping Chen, Chih-Heng Hsieh, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1. Taiwan J Obstet Gynecol 2017; 56: 847-851.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Li-Feng Chen, Wayseen Wang. Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis. Taiwan J Obstet Gynecol 2017; 56: 852-856.

Chih-Ping Chen, Tung-Yao Chang, Tan-Wei Lin, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wayseen Wang. Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasia. Taiwan J Obstet Gynecol 2018; 57: 119-122.

Chih-Ping Chen, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wayseen Wang. Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus. Taiwan J Obstet Gynecol 2018; 57: 123-127.

Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Chen-Chi Lee, Wayseen Wang. Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities. Taiwan J Obstet Gynecol 2018; 57: 128-132.

Shih-Ting Lai, Chih-Ping Chen, Chen-Ju Lin, Chin-Yuan Hsu, Peih-Shan Wu, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang. Late-onset fetal bilateral pleural effusions associated with Down syndrome. Taiwan J Obstet Gynecol 2018; 57: 133-136.

Peng-Hui Wang, Chih-Ping Chen, Tsung-Cheng Kuo. Outstanding research paper awards of the 2017 Taiwanese Journal of Obstetrics and Gynecology. Taiwan J Obstet Gynecol 2018; 57: 177-178.

Peng-Hui Wang, Chih-Ping Chen, Tsung-Cheng Kuo. Outstanding female cancer research paper awards of the 2017 Taiwanese Journal of Obstetrics and Gynecology. Taiwan J Obstet Gynecol 2018; 57: 179.

Chen-Ju Lin, Shin-Wen Chen, Chih-Ping Chen, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, L i-Feng Chen, Meng-Shan Lee, Chen-Wen Pan, Ku-Chien Lin, Tze-Tien Yeh. Higher male prevalence of chromosomal mosaicism detected by amniocentesis. Taiwan J Obstet Gynecol 2018; 57: 370-373.

Shih-Ting Lai, Chih-Ping Chen, Chen-Ju Lin, Yen-Ni Chen, Shin-Wen Chen. Reply to comment on An intrauterine gestational sac surrounded by thin myometrium at fundus. J Med Ultrasound 2018; 26: 170.

Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wen-Lin Chen, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability. Taiwan J Obstet Gynecol 2018; 57: 578-582.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wen-Lin Chen, Wayseen Wang. A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows. Taiwan J Obstet Gynecol 2018; 57: 583-587.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Li-Feng Chen, Wayseen Wang. A 17-year-old boy with Klinefelter syndrome presenting Marfan syndrome-like clinical features of tall stature, scoliosis, arachnodactyly and subluxation of bilateral elbow joints. Taiwan J Obstet Gynecol 2018; 57: 608-610.

Chih-Ping Chen, Shu-Yuan Chang, Liang-Kai Wang, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Dai-Dyi Town, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound. Taiwan J Obstet Gynecol 2018; 57: 730-733.

Chih-Ping Chen, Shu-Yuan Chang, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wen-Lin Chen, Chien-Wen Yang, Wayseen Wang. Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound. Taiwan J Obstet Gynecol 2018; 57: 734-738.

Chih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound. Taiwan J Obstet Gynecol 2018; 57: 739-744.

Chih-Ping Chen, Shu-Yuan Chang, Hui-Shuan Lau, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Meng-Shan Lee, Wayseen Wang. First-trimester cystic hygroma and omphalocele in a fetus with Turner syndrome. Taiwan J Obstet Gynecol 2018; 57: 763-764.

Chih-Ping Chen, Shu-Yuan Chang, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wen-Lin Chen, Wayseen Wang. Array comparative genomic hybridization characterization of a 3.3-Mb 17p13.3-p13.2 deletion encompassing YWHAE, CRK, HIC1 and PAFAH1B1 in an 8-year-old girl with Miller-Dieker lissencephaly syndrome, congenital heart defects, growth restriction and developmental delay. Taiwan J Obstet Gynecol 2018; 57: 765-768.

Chih-Ping Chen, Shu-Yuan Chang, Ming-Chao Huang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wayseen Wang. Detection of hypomethylation of H19 in a pregnancy with limb-body wall complex. Taiwan J Obstet Gynecol 2018; 57: 769-771.

Tzu-Yun Chuang, Shu-Yuan Chang, Chih-Ping Chen, Ming-Huei Lin, Cheng-Yu Chen, Shin-Wen Chen, Schu-Rern Chern, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang. Digynic triploidy in a fetus presenting with semilobar holoprosencephaly. Taiwan J Obstet Gynecol 2018; 57: 881-884.

Peng-Hui Wang, Chih-Ping Chen, Tsung-Cheng Kuo. Outstanding research paper awards of the 2018 Taiwanese Journal of Obstetrics and Gynecology. Taiwan J Obstet Gynecol 2019; 58: 309-310.

Peng-Hui Wang, Pei-Fen Lo, Chih-Ping Chen. Outstanding female cancer research paper awards of the 2018 Taiwanese Journal of Obstetrics and Gynecology. Taiwan J Obstet Gynecol 2019; 58: 311-312.

Chih-Ping Chen, Ming-Chao Huang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Tzu-Yun Chuang, Dai-Dyi Town, Wayseen Wang. Mosaic trisomy 22 at amniocentesis: prenatal diagnosis and literature review. Taiwan J Obstet Gynecol 2019; 58: 692-697.

Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang. Inv dup del(10p): prenatal diagnosis and molecular cytogenetic characterization. Taiwan J Obstet Gynecol 2019; 58: 698-703.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang. Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects Taiwan J Obstet Gynecol 2019; 58: 704-708.

Chung-Lin Lee, Chen-Hao Lee, Chih-Kuang Chuang, Huei-Ching Chiu, Yen-Jiun Chen, Chao-Ling Chou, Peih-Shan Wu, Chih-Ping Chen, Hsiang-Yu Lin, Shuan-Pei Lin. Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan. Pediatr Neonatol 2019; 60: 453-460.

Chih-Ping Chen, Fang-Yu Hung, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2019; 58: 852-854.

Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang. Mosaic isochromosome 20q at amniocentesis: prenatal diagnosis, genetic counseling and literature review. Taiwan J Obstet Gynecol 2019; 58: 855-858.

Chih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Wayseen Wang, Chen-Chi Lee. Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound. Taiwan J Obstet Gynecol 2019; 58: 859-863.

Chih-Ping Chen, Tsang-Ming Ko, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3. Taiwan J Obstet Gynecol 2019; 58: 864-868.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Tzu-Yun Chuang, Wayseen Wang. Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects. Taiwan J Obstet Gynecol 2019; 58: 869-871.

Chih-Ping Chen, Chin-Yuan Hsu, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Wayseen Wang. Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum. Taiwan J Obstet Gynecol 2020; 59: 127-129.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis. Taiwan J Obstet Gynecol 2020; 59: 130-134.

Chih-Ping Chen, Jian-Pei Huang, Shin-Wen Chen, Schu-Rern Chern, Peih-Shan Wu, Fang-Tzu Wu, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects. Taiwan J Obstet Gynecol 2020; 59: 135-139.

Chih-Ping Chen, Jian-Pei Huang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication. Taiwan J Obstet Gynecol 2020; 59: 140-145.

Chih-Ping Chen, Yi-Hui Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Meng-Shan Lee, Yun-Yi Chen, Wayseen Wang. Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesi. Taiwan J Obstet Gynecol 2020; 59: 146-149.

Chih-Ping Chen, Shin-Yu Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2020; 59: 301-305.

Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang. Monozygotic twins discordant for low-level mosaic trisomy 17 at amniocentesis in a pregnancy with a favorable outcome and a literature review of heterokaryotypic monozygotic twins at amniocentesis. Taiwan J Obstet Gynecol 2020; 59: 306-313.

Chih-Ping Chen, Yu-Ling Kuo, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2020; 59: 327-330.

Chih-Ping Chen, Shun-Long Weng, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis of mosaicism for trisomy 11 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2020; 59: 331-333.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis of mosaicism for a distal 5p deletion in a single colony at amniocentesis in a pregnancy with a favorable outcome and a review of mosaic distal 5p deletion. Taiwan J Obstet Gynecol 2020; 59: 334-337.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Yun-Yi Chen, Wayseen Wang. Wolf-Hirschhorn syndrome: prenatal diagnosis and molecular cytogenetic characterization of a de novo distal deletion of 4p (4p16.1→pter) in a fetus with facial cleft and preaxial polydactyly. Taiwan J Obstet Gynecol 2020; 59: 425-431.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletion. Taiwan J Obstet Gynecol 2020; 59: 432-436.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interchromosomal insertion of ins(1;8)(p22.1;q22q23). Taiwan J Obstet Gynecol 2020; 59: 437-439.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Wayseen Wang. Perinatal cytogenetic discrepancy in a fetus with low-level mosaicism for trisomy 21 and a favorable outcome. Taiwan J Obstet Gynecol 2020; 59: 440-442.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Wayseen Wang. Prenatal diagnosis of mosaicism for double trisomies of trisomy 11 and trisomy 12 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2020; 59: 443-445.

Peng-Hui Wang, Chih-Ping Chen, Ming-Chao Huang. Introduce the outstanding research paper awards of the Taiwan Association of Obstetrics and Gynecology and Hsu Chien-Tien Cancer Foundation in 2020. Taiwan J Obstet Gynecol 2020; 59: 477-478.

Chih-Ping Chen, Hsiang-Yu Lin, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Sisca Fran, Yun-Yi Chen, Dai-Dyi Town, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15). Taiwan J Obstet Gynecol 2020; 59: 580-585.

Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound. Taiwan J Obstet Gynecol 2020; 59: 598-603.

Chih-Ping Chen, Chao-Yun Wu, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Yun-Yi Chen, Wayseen Wang. Prenatal diagnosis of mosaicism for trisomy 12 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2020; 59: 604-606.

Chih-Ping Chen, Schu-Rern Chern, Liang-Kai Wang, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang. Detection of paternal origin of fetal trisomy 18 in a pregnancy conceived by assisted reproductive technology and in vitro fertilization. Taiwan J Obstet Gynecol 2020; 59: 607-609.

Chih-Ping Chen, Wan-Chun Huang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Meng-Shan Lee, Wayseen Wang. Detection of paternal origin of fetal trisomy 21 in a pregnancy with isolated ventriculomegaly but without advanced parental age. Taiwan J Obstet Gynecol 2020; 59: 610-612.

Chih-Ping Chen, Te-Yao Hsu, Tsang-Ming Ko, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis. Taiwan J Obstet Gynecol 2020; 59: 728-735.

Chih-Ping Chen, Tsang-Ming Ko, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Wen-Lin Chen, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome. Taiwan J Obstet Gynecol 2020; 59: 754-757.

Chih-Ping Chen, Jui-Der Liou, Kok-Min Seow, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results. Taiwan J Obstet Gynecol 2020; 59: 758-762.

Chih-Ping Chen, Chin-Yuan Hsu, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang. Prenatal diagnosis of a 1.651-Mb 19q13.42-q13.43 microdeletion in a fetus with micrognathia and bilateral pyelectasis on prenatal ultrasound. Taiwan J Obstet Gynecol 2020; 59: 763-765.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin. Taiwan J Obstet Gynecol 2020; 59: 766-769.

Chih-Ping Chen, Tsang-Ming Ko, Jian-Pei Huang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis of a familial normal euchromatic variant of dup(15)(q11.2q11.2) in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2020; 59: 770-772.

Chih-Ping Chen, Schu-Rern Chern, Fang-Tzu Wu, Yun-Yi Chen, Meng-Shan Lee, Wayseen Wang. Low-level mosaic trisomy 13 at amniocentesis associated with a favorable outcome in a pregnancy. Taiwan J Obstet Gynecol 2020; 59: 935-937.

Chih-Ping Chen, Schu-Rern Chern, Liang-Kai Wang, Peih-Shan Wu, Fang-Tzu Wu, Yun-Yi Chen, Dai-Dyi Town, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy. Taiwan J Obstet Gynecol 2020; 59: 938-940.

Chih-Ping Chen, Chen-Ju Lin, Shin-Wen Chen, Fang-Tzu Wu, Schu-Rern Chern, Peih-Shan Wu, Yun-Yi Chen, Wen-Lin Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia. Taiwan J Obstet Gynecol 2020; 59: 941-944.

Chih-Ping Chen, Steven W. Shaw, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang. Prenatal diagnosis and management of monozygotic twins discordant for severe fetal abnormalities. Taiwan J Obstet Gynecol 2020; 59: 945-947.

Chih-Ping Chen. Low-level mosaic tetrasomy 18p at amniocentesis can be associated with a favorable pediatric outcome: the follow-ups of three consecutive cases. Taiwan J Obstet Gynecol 2020; 59: 985-986.

Chih-Ping Chen, Chia-Hao Chan, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome. Taiwan J Obstet Gynecol 2021; 60: 152-156.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion. Taiwan J Obstet Gynecol 2021; 60: 157-160.

Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang. Prenatal diagnosis of familial 2p15 microduplication associated with pulmonary artery stenosis, single umbilical artery and left foot postaxial polydactyly on fetal ultrasound. Taiwan J Obstet Gynecol 2021; 60: 161-164.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang. Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother. Taiwan J Obstet Gynecol 2021; 60: 165-168.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang. Tetrasomy of 11q13.4-q14.3 due to an intrachromosomal triplication associated with paternal uniparental isodisomy for 11q14.3-qter, intrauterine growth restriction, developmental delay, corpus callosum dysgenesis, microcephaly, congenital heart defects and facial dysmorphism. Taiwan J Obstet Gynecol 2021; 60: 169-172.

Chih-Ping Chen, Liang-Ming Lo, Tsang-Ming Ko, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Li-Feng Chen, Yun-Yi Chen, Wayseen Wang. Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes. Taiwan J Obstet Gynecol 2021; 60: 331-334.

Chih-Ping Chen, Ming-Huei Lin, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome. Taiwan J Obstet Gynecol 2021; 60: 335-340.

Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang. Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autism and congenital heart defects. Taiwan J Obstet Gynecol 2021; 60: 341-344.

Chih-Ping Chen, Ming Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Gwo-Chin Ma, Shun-Ping Chang, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Yun-Yi Chen, Wayseen Wang. Low-level mosaicism for trisomy 16 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome. Taiwan J Obstet Gynecol 2021; 60: 345-349.

Shih-Ting Lai, Chih-Ping Chen, Chen-Ju Lin, Shin-Wen Chen, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis of persistent left superior vena cava, polyhydramnios and a small gastric bubble in a fetus with VACTERL association. Taiwan J Obstet Gynecol 2021; 60: 355-358.

Chih-Ping Chen. Disappearance of the trisomy 15 cell line at long-term follow-up in mosaic trisomy 15 at amniocentesis. Taiwan J Obstet Gynecol 2021; 60: 373.

Chih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Dai-Dyi Town, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus. Taiwan J Obstet Gynecol 2021; 60: 534-539.

Chih-Ping Chen, Cheng-En Hsieh, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis of trisomy 11 in a single colony of cultured amniocytes at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2021; 60: 540-542.

Chih-Ping Chen, Hsiu-Ting Tsai, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Dai-Dyi Town, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis of mosaicism for double aneuploidy of 47,XXY and trisomy 7 (48,XXY,+7) at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2021; 60: 543-548.

Chih-Ping Chen, Shih-Shien Weng, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang. Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly, ventricular septal defect, arthrogryposis of bilateral wrists and aplasia of the thumbs Taiwan J Obstet Gynecol 2021; 60: 549-550.

Peng-Hui Wang, Chih-Ping Chen, Ming-Chao Huang. Introduce the outstanding research paper awards of the Taiwan Association of Obstetrics and Gynecology in 2020. Taiwan J Obstet Gynecol 2021; 60: 591-592.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang. Prenatal diagnosis of recurrent mosaic ring chromosome 13 of maternal origin. Taiwan J Obstet Gynecol 2021; 60: 771-774.

Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result. Taiwan J Obstet Gynecol 2021; 60: 775-777.

Chih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Meng-Shan Lee, Wayseen Wang. Mosaic Xq duplication, or 46,X,der(X)dup(X)(q22.1q22.2)dup(X)(q25q22.3)/46,XX at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2021; 60: 778-780.

Chih-Ping Chen, Pu-Tsui Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang. Prenatal diagnosis of a familial Y long-arm and chromosome 15 short-arm translocation inherited from a mother carrier. Taiwan J Obstet Gynecol 2021; 60: 781-783.

Chih-Ping Chen. Low-level mosaic trisomy 17 at amniocentesis can be associated with a favorable pediatric outcome: the follow-ups of three consecutive cases. Taiwan J Obstet Gynecol 2021; 60: 794-795.

Peng-Hui Wang, Chih-Ping Chen. A new hope or a new nightmare? Concerned about the conflicted data. Taiwan J Obstet Gynecol 2021; 60: 799-800.

Chih-Ping Chen, Chao-Yun Wu, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Mang-Shang Lee, Wayseen Wang. Rapid diagnosis of trisomy 13 of maternal origin by quantitative fluorescent polymerase chain reaction analysis in a pregnancy with fetal holoprosencephaly, premaxillary agenesis, postaxial polydactyly of left hand and overriding aorta. Taiwan J Obstet Gynecol 2021; 60: 903-904.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis of a familial 9p12 amplification inherited from a father carrier. Taiwan J Obstet Gynecol 2021; 60: 905-906.

Chih-Ping Chen. Disappearance of the trisomy 8 cell line at long-term follow-up in mosaic trisomy 8 at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2021; 60: 949-950.

Chih-Ping Chen, Schu-Rern Chern, Chien-Hsing Lin, Chin-Yuan Hsu, Hsiang-Yu Lin, Fang-Tzu Wu, Shin-Wen Chen, Wayseen Wang. Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndrome. Taiwan J Obstet Gynecol 2021; 60: 1103-1106.

Chih-Ping Chen, Fei-Hua Lan, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Mang-Shang Lee, Chen-Wen Pan, Yun-Yi Chen, Wayseen Wang. Prenatal diagnosis of mosaic trisomy 16 by amniocentesis in a pregnancy associated with abnormal first-trimester screening result (low PAPP-A and low PlGF), intrauterine growth restriction and a favorable outcome. Taiwan J Obstet Gynecol 2021; 60: 1107-1111.

Chih-Ping Chen, Schu-Rern Chern, Chien-Hsing Lin, Chin-Yuan Hsu, Hsiang-Yu Lin, Fang-Tzu Wu, Shin-Wen Chen, Wayseen Wang. Application of array comparative genomic hybridization analysis for rapid differential diagnosis of a chromosome euchromatic variant of dup 22q13.3 at amniocentesis. Taiwan J Obstet Gynecol 2021; 60: 1134-1135.

Chih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis of mosaicism for trisomy 11 in a single colony at amniocentesis in a twin pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2021; 60: 1136-1138.

Chih-Ping Chen, Wen-Chu Huang, Schu-Rern Chern, Fang-Tzu Wu, Shin-Wen Chen, Dai-Dyi Town, Wayseen Wang. Detection of placental mosaic trisomy 17 in a pregnancy associated with mosaicism for trisomy 17 in a single colony at amniocentesis with a favorable outcome. Taiwan J Obstet Gynecol 2021; 60: 1139-1141.

Chung-Lin Lee, Chih-Kuang Chuang, Ru-Yi Tu, Huei-Ching Chiu, Yun-Ting Lo, Ya-Hui Chang, Yen-Jiun Chen, Chao-Ling Chou, Peih-Shan Wu, Chih-Ping Chen, Hsiang-Yu Lin, Shuan-Pei Lin. Increased diagnostic yield of array comparative genomic hybridization for autism spectrum disorder in one institution in Taiwan. Medicina (Kaunas) 2022; 58: 15.

Chih-Ping Chen, Ming Chen, Gwo-Chin Ma, Shun-Ping Chang, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Mang-Shang Lee, Wayseen Wang. Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14)(q10;q10). Taiwan J Obstet Gynecol 2022; 61: 132-134.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Shin-Yin Huang, Wayseen Wang. Application of quantitative fluorescent polymerase chain reaction analysis for the rapid confirmation of trisomy 13 of maternal origin in a pregnancy with fetal holoprosencephaly, cyclopia, polydactyly, omphalocele and cell culture failure. Taiwan J Obstet Gynecol 2022; 61: 135-137.

Chih-Ping Chen, Yi-Hui Lin, Peih-Shan Wu, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Chen-Wen Pan, Yun-Yi Chen, Wayseen Wang. Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2022; 61: 138-140.

Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Yun-Yi Chen, Wayseen Wang. Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcome. Taiwan J Obstet Gynecol 2022; 61: 141-145.

Chih-Ping Chen, Jui-Der Liou, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Meng-Shan Lee, Yun-Yi Chen, Wayseen Wang. Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome. Taiwan J Obstet Gynecol 2022; 61: 146-149.

Shu-Chin Chien, Chih-Ping Chen, Jui-Der Liou. Prenatal diagnosis and genetic counseling of uniparental disomy. Taiwan J Obstet Gynecol 2022; 61: 210-215.

Chih-Ping Chen, Quan-Bin Jou, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Wayseen Wang. Detection of paternal origin of fetal de novo rea(21q;21q) Down syndrome in a pregnancy of a young woman associated with an abnormal first-trimester maternal serum screening result. Taiwan J Obstet Gynecol 2022; 61: 356-358.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 21 associated with low PAPP-A and low PlGF in the first-trimester maternal serum screening. Taiwan J Obstet Gynecol 2022; 61: 359-363.

Chih-Ping Chen, Ming Chen, Gwo-Chin Ma, Shun-Ping Chang, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Meng-Shan Lee, Yun-Yi Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22. Taiwan J Obstet Gynecol 2022; 61: 364-367.

Chih-Ping Chen, Jun-Wei Su, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang. Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic 46,XX,dup(9)(q22.3q34.1)/46,XX at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2022; 61: 368-371.

Chih-Ping Chen, Chao-Yun Wu, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Yun-Yi Chen, Li-Feng Chen, Wayseen Wang. Perinatal cytogenetic discrepancy in a pregnancy with mosaic 45,X/46,XY at amniocentesis and a favorable outcome. Taiwan J Obstet Gynecol 2022; 61: 525-527.

Chih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Li-Feng Chen, Yun-Yi Chen, Wayseen Wang. High-level mosaicism for 45,X in 45,X/46,X,idic(Y)(q11.2) at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line. Taiwan J Obstet Gynecol 2022; 61: 528-531.

Chih-Ping Chen, Shin-Wen Chen, Peih-Shan Wu, Fang-Tzu Wu, Wayseen Wang. A false-positive result at non-invasive prenatal testing due to maternal 17p12 microduplication. Taiwan J Obstet Gynecol 2022; 61: 532-534.

Chih-Ping Chen. Low-level mosaic trisomy 21 at amniocentesis can be associated with a favorable pediatric outcome: The follow-up of a child at age 6 years and 4 months. Taiwan J Obstet Gynecol 2022; 61: 557.

Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis of mosaicism for trisomy 17 in a single colony at amniocentesis with a negative non-invasive prenatal testing (NIPT) result in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2022; 61: 558-559.

Chih-Ping Chen. Detection of maternal origin of fetal trisomy 18 in a pregnancy with incidental detection of low-level mosaicism for X aneuploidy in a 46-year-old woman. Taiwan J Obstet Gynecol 2022; 61: 560-561.

Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis of pseudomosaicism for trisomy 20 at amniocentesis with a negative non-invasive prenatal testing (NIPT) result in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2022; 61: 675-676.

Chih-Ping Chen, Tsang-Ming Ko, Tze-Chien Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Yun-Yi Chen, Wayseen Wang. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2022; 61: 677-683.

Chih-Ping Chen, Jun-Wei Su, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Meng-Shan Lee, Chen-Wen Pan, Yun-Yi Chen, Wayseen Wang. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 18 at amniocentesis in a pregnancy with a favorable fetal outcome and maternal uniparental disomy 18. Taiwan J Obstet Gynecol 2022; 61: 684-689.

Chih-Ping Chen, Te-Yao Hsu, Ching-Chang Tsai, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Peih-Shan Wu, Chen-Chi Lee, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang. Mosaic trisomy 18 at amniocentesis associated with a favorable fetal outcome in a pregnancy. Taiwan J Obstet Gynecol 2022; 61: 690-694.

Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Chen-Wen Pan, Yun-Yi Chen, Wayseen Wang. High-level mosaicism for 45,X in 45,X/46,XY at amniocentesis in a pregnancy with a favorable fetal outcome and cytogenetic discrepancy in various tissues. Taiwan J Obstet Gynecol 2022; 61: 695-699.

Chih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Yun-Yi Chen, Wayseen Wang. High-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line. Taiwan J Obstet Gynecol 2022; 61: 700-702.

Shin-Wen Chen, Chih-Ping Chen, Schu-Rern Chern, Yu-Ling Kuo, Chien-Ling Chiu. The significance of karyotyping and azoospermia factor analysis in patients with nonobstructive azoospermia or oligozoospermia. Taiwan J Obstet Gynecol 2022; 61: 800-805.

Chih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Wen-Lin Chen, Yun-Yi Chen, Wayseen Wang. Detection of mosaicism for 46,X,i(Y)(q10) in the blood lymphocytes in a phenotypically normal male neonate with prenatally detected 45,X/46,XY at amniocentesis and cytogenetic discrepancy in various tissues. Taiwan J Obstet Gynecol 2022; 61: 873-875.

Chih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Wen-Lin Chen, Yun-Yi Chen, Wayseen Wang. Progressive increase of the mosaic level for 45,X in 45,X/46,XX at different amniocenteses and postnatal progressive decrease of the 45,X cell line in a mosaic 45,X/46,XX fetus with a favorable outcome. Taiwan J Obstet Gynecol 2022; 61: 876-879.

Yu-Min Syu, Juine-Yih Ma, Tzu-Hsuen Ou, Chung-Lin Lee, Hsiang-Yu Lin, Shuan-Pei Lin, Chia-Jung Lee, Chih-Ping Chen. De Novo Mosaic 6p23-p25.3 tetrasomy caused by a small supernumerary marker chromosome presenting trisomy distal 6p phenotype: A case report and literature review. Diagnostics 2022; 12: 2306.

Chih-Ping Chen, Shyr-Yeu Lin, Chii-Ruey Tzeng, Liang-Kai Wang, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang. Late amniocentesis with uniparental disomy testing following successful in vitro fertilization and transfer of three mosaic embryos in a pregnancy with a favorable outcome. Taiwan J Obstet Gynecol 2022; 61: 1037-1038.

Chih-Ping Chen, Shin-Wen Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a de novo deletion of 4q34.1→qter associated with low PAPP-A and low PlGF in the first-trimester maternal serum screening, congenital heart defect on fetal ultrasound and a false negative non-invasive prenatal testing (NIPT) result. Taiwan J Obstet Gynecol 2022; 61: 1037-1038.

Chih-Ping Chen, Shin-Wen Chen, Schu-Rern Chern, Peih-Shan Wu, Fang-Tzu Wu, Yen-Ting Pan, Chen-Wen Pan, Wayseen Wang. Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 2q12.2→q13 encompassing MALL, NPHP1, RGPD6 and BUB1. Taiwan J Obstet Gynecol 2022; 61: 1039-1043.

Chih-Ping Chen, Shin-Wen Chen, Jain-Pei Huang, Schu-Rern Chern, Fang-Tzu Wu, Yen-Ting Pan, Chen-Chi Lee, Wayseen Wang. Rapid confirmation of trisomy 13 of maternal origin by QF-PCR following postmortem tissue cell culture failure in a pregnancy with trisomy 13 at amniocentesis and fetal postaxial polydactyly and facial cleft. Taiwan J Obstet Gynecol 2022; 61: 1048-1052.

Chih-Ping Chen, Shin-Wen Chen, Chi-Kang Lin, Fang-Tzu Wu, Yun-Yi Chen, Li-Feng Chen, Wayseen Wang. 45,X/46,XX at amniocentesis associated with a favorable outcome and postnatal decrease of the 45,X cell line. Taiwan J Obstet Gynecol 2022; 61: 1086-1087.

Chih-Ping Chen, Shin-Wen Chen, Fang-Tzu Wu, Yen-Ting Pan, Wayseen Wang. Spontaneous resolution of septated cystic hygroma with a severely increased nuchal translucency thickness of 5.8 mm detected in the first-trimester in a pregnancy with no abnormalities in chromosomal, microarray and whole exome sequencing analyses and a favorable fetal outcome. Taiwan J Obstet Gynecol 2022; 61: 1088-1089.