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Taiwanese Journal of Obstetrics & Gynecology|November 25, 2019
Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen, Fang-Yu Hung, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 25, 2019
Mosaic isochromosome 20q at amniocentesis: Prenatal diagnosis, genetic counseling and literature reviewChih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 25, 2019
Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defectsChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 26, 2023
The correlation with abnormal fetal outcome and a high level of amniotic fluid alpha-fetoprotein in mid-trimesterTian-Jeau Huang, Chih-Ping Chen, Chen-Ju Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 5, 2020
Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen, Shin-Yu Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 5, 2020
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 amniocentesisChih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 19, 2021
Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndromeChih-Ping Chen, Schu-Rern Chern, Chien-Hsing Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 4, 2017
Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorderChih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 25, 2022
Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 2q12.2→q13 encompassing MALL, NPHP1, RGPD6 and BUB1Chih-Ping Chen, Shin-Wen Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 25, 2022
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 cleftChih-Ping Chen, Shin-Wen Chen, Jain-Pei Huang, et al.
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