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Taiwanese Journal of Obstetrics & Gynecology|January 26, 2021
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndromeChih-Ping Chen, Chia-Hao Chan, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 26, 2021
Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletionChih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 23, 2019
Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterizationChih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 2, 2017
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disabilityChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 4, 2017
Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3Shin-Wen Chen, Chih-Ping Chen, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 1, 2022
Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 21 associated with low PAPP-A and low PlGF in the first-trimester maternal serum screeningChih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 18, 2020
Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletionChih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 21, 2018
A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbowsChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 20, 2022
Perinatal cytogenetic discrepancy in a pregnancy with mosaic 45,X/46, XY at amniocentesis and a favorable outcomeChih-Ping Chen, Chao-Yun Wu, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 21, 2020
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasiaChih-Ping Chen, Chen-Ju Lin, Shin-Wen Chen, et al.
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