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Taiwanese Journal of Obstetrics & Gynecology|July 12, 2021
Prenatal diagnosis of recurrent mosaic ring chromosome 13 of maternal originChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 21, 2018
Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasiaChih-Ping Chen, Tung-Yao Chang, Tan-Wei Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 23, 2019
Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature reviewChih-Ping Chen, Ming-Chao Huang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 25, 2023
Low-level mosaic trisomy 15 at amniocentesis without uniparental disomy 15 in a pregnancy associated with cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes, a favorable fetal outcome and perinatal decrease of the aneuploid cell lineChih-Ping Chen, Shin-Wen Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 15, 2023
Prenatal diagnosis and molecular genetic analysis of recurrent trisomy 18 of maternal origin in two consecutive pregnanciesChih-Ping Chen, Fang-Tzu Wu, Chian-Huey Wong, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 25, 2022
Late amniocentesis with uniparental disomy testing following successful in vitro fertilization and transfer of three mosaic embryos in a pregnancy with a favorable outcomeChih-Ping Chen, Shyr-Yeu Lin, Chii-Ruey Tzeng, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 25, 2019
Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasoundChih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 21, 2018
Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetusChih-Ping Chen, Tsang-Ming Ko, Tung-Yao Chang, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 18, 2020
Prenatal diagnosis of mosaicism for double trisomies of trisomy 11 and trisomy 12 in a single colony at amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 11, 2020
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesisChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
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