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Taiwanese Journal of Obstetrics & Gynecology|February 11, 2020
Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defectsChih-Ping Chen, Jian-Pei Huang, Shin-Wen Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 11, 2020
Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesisChih-Ping Chen, Yi-Hui Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 25, 2023
Low-level mosaic trisomy 17 at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy between cultured and uncultured amniocytesChih-Ping Chen, Shin-Wen Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|June 11, 2017
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11Chih-Ping Chen, Ming Chen, Pu-Tsui Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 4, 2016
Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplicationChih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|December 16, 2017
Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bonesChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 19, 2016
Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature reviewChih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 13, 2020
Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasoundChih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 2, 2022
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen, Tsang-Ming Ko, Tze-Chien Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 20, 2017
Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormalityChih-Ping Chen, Schu-Rern Chern, Yen-Ni Chen, et al.
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