生育保健學科暨遺傳諮詢中心

專書:

2. Chih-Ping Chen. Prenatal diagnosis and genetic counseling of omphalocele: an overview and atlas of cases. Elsevier Taiwan LLC, 2007.  ISBN 978-986-83792-0-6.
4. Chih-Ping Chen.  Prenatal diagnosis and genetic counseling of neural tube defects: an overview and atlas of cases. Elsevier Taiwan LLC, 2009.  ISBN 978-986-6538-23-0.

論文研究(2015年):

2. 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 fluorescence 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.
4. 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.
6. 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.