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Taiwanese Journal of Obstetrics & Gynecology|July 2, 2022
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 18 at amniocentesis in a pregnancy with a favorable fetal outcome and maternal uniparental disomy 18Chih-Ping Chen, Jun-Wei Su, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 2, 2022
Mosaic trisomy 18 at amniocentesis associated with a favorable fetal outcome in a pregnancyChih-Ping Chen, Te-Yao Hsu, Ching-Chang Tsai, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 22, 2018
Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasoundChih-Ping Chen, Shu-Yuan Chang, Chen-Ju Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 15, 2023
Molecular cytogenetic characterization of del(X)(p22.33)mat and de novo dup(4)(q34.3q35.2) in a male fetus with multiple anomalies of facial dysmorphism, ventriculomegaly, congenital heart defects, short long bones and clinodactylyChih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 10, 2021
Prenatal diagnosis of mosaicism for double aneuploidy of 47,XXY and trisomy 7 (48,XXY,+7) at amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen, Hsiu-Ting Tsai, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 21, 2018
Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalitiesChih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 8, 2021
Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndromeChih-Ping Chen, Ming-Huei Lin, Yi-Yung Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 19, 2016
Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversionChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 1, 2022
Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic 46,XX,dup(9)(q22.3q34.1)/46,XX at amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen, Jun-Wei Su, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 31, 2023
Mosaic trisomy 21 at amniocentesis in a twin pregnancy associated with a favorable fetal outcome, maternal uniparental disomy 21 and postnatal decrease of the trisomy 21 cell lineChih-Ping Chen, Te-Yao Hsu, Schu-Rern Chern, et al.
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