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Taiwanese Journal of Obstetrics & Gynecology|May 15, 2023
Low-level mosaic trisomy 9 at amniocentesis associated with a positive non-invasive prenatal testing for trisomy 9, maternal uniparental disomy 9, intrauterine growth restriction and a favorable fetal outcome in a pregnancyChih-Ping Chen, Tsang-Ming Ko, Shin-Wen Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 25, 2019
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3Chih-Ping Chen, Tsang-Ming Ko, Chen-Yu Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 20, 2017
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcomeChih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|June 11, 2017
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 syndromeChih-Ping Chen, Chang-Sheng Yin, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 4, 2016
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 amniocentesisChih-Ping Chen, Shing-Jyh Chang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|December 16, 2017
Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcomeChih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 19, 2022
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 outcomeChih-Ping Chen, Jui-Der Liou, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 21, 2018
Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disabilityChih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 15, 2017
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16Chih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 12, 2021
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 outcomeChih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, et al.
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