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Taiwanese Journal of Obstetrics & Gynecology|April 20, 2017
Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosisChih-Ping Chen, Kuo-Gon Wang, Hsu-Kuang Huang, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 25, 2023
Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy in various tissuesChih-Ping Chen, Shun-Long Weng, Shin-Wen Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 10, 2021
Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetusChih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 31, 2023
Molecular cytogenetic characterization of de novo concomitant proximal 21q deletion of 21q11.2q21.3 and distal Xp deletion of Xp22.33p22.2 due to an unbalanced X;21 translocation detected by amniocentesisChih-Ping Chen, Shin-Wen Chen, Chao-Yun Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 31, 2023
Molecular cytogenetic characterization of de novo concomitant distal 8p deletion of 8p23.3p23.1 and Xp and Xq deletion of Xp22.13q28 due to an unbalanced X;8 translocation detected by amniocentesisChih-Ping Chen, Fang-Yu Hung, Shin-Wen Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 31, 2023
Mosaic tetrasomy 9p at amniocentesis in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the aneuploid cell line and cytogenetic discrepancy in various tissuesChih-Ping Chen, Shin-Wen Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 30, 2016
Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytesChih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 12, 2020
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 resultsChih-Ping Chen, Jui-Der Liou, Kok-Min Seow, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 12, 2020
Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal originChih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 12, 2020
Prenatal diagnosis of a familial normal euchromatic variant of dup(15)(q11.2q11.2) in a pregnancy with a favorable outcomeChih-Ping Chen, Tsang-Ming Ko, Jian-Pei Huang, et al.
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