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Taiwanese Journal of Obstetrics & Gynecology|September 10, 2022
Progressive increase of the mosaic level for 45,X in 45,X/46, XX at different amniocenteses and postnatal progressive decrease of the 45,X cell line in a mosaic 45,X/46, XX fetus with a favorable outcomeChih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|June 11, 2017
Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1Chih-Ping Chen, Hoi-Kin Yip, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 13, 2020
Prenatal diagnosis of mosaicism for trisomy 12 in a single colony at amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen, Chao-Yun Wu, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 5, 2020
Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen, Yu-Ling Kuo, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 5, 2020
Prenatal diagnosis of mosaicism for a distal 5p deletion in a single colony at amniocentesis in a pregnancy with a favorable outcome and a review of mosaic distal 5p deletionChih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 20, 2022
High-level mosaicism for 45,X in 45,X/46,X,idic(Y)(q11.2) at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell lineChih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 23, 2019
Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defectsChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 4, 2017
Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delayChih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 26, 2021
Tetrasomy of 11q13.4-q14.3 due to an intrachromosomal triplication associated with paternal uniparental isodisomy for 11q14.3-qter, intrauterine growth restriction, developmental delay, corpus callosum dysgenesis, microcephaly, congenital heart defects and facial dysmorphismChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 19, 2022
Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcomeChih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, et al.
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