台兒TMAMA

編號： 11
2015/02 Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma
作者：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
發表期刋： Taiwanese Journal of Obstetrics and Gynecology , Volume 54 , Issue 1 , 78 - 80

編號： 12
2014/06 Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects
作者：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 Chang
發表期刋： Taiwanese Journal of Obstetrics and Gynecology , Volume 53 , Issue 2 , 248 - 251

編號： 13
2014/03 Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith–Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer
作者：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
發表期刋： Taiwanese Journal of Obstetrics and Gynecology , Volume 53 , Issue 1 , 90 - 94

編號： 14
2013/12 VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer
作者：Chih-Ping Chen, Tung-Yao Chang, Yi-Yung Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang
發表期刋： Taiwanese Journal of Obstetrics and Gynecology , Volume 52 , Issue 4 , 575 - 579

編號： 15
2013/12 Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review
作者：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
發表期刋： Gene, Volume 532, Issue 1, 2013, Pages 152-159

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