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Taiwanese Journal of Obstetrics & Gynecology|July 2, 2022
Prenatal diagnosis of pseudomosaicism for trisomy 20 at amniocentesis with a negative non-invasive prenatal testing (NIPT) result in a pregnancy with a favorable outcomeChih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 2, 2022
High-level mosaicism for 45,X in 45,X/46, XY at amniocentesis in a pregnancy with a favorable fetal outcome and cytogenetic discrepancy in various tissuesChih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|June 11, 2017
Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucencyChih-Ping Chen, Chen-Ju Lin, Yen-Ni Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 11, 2020
Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplicationChih-Ping Chen, Jian-Pei Huang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|May 18, 2020
Wolf-Hirschhorn syndrome: Prenatal diagnosis and molecular cytogenetic characterization of a de novo distal deletion of 4p (4p16.1 → pter) in a fetus with facial cleft and preaxial polydactylyChih-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 de novo interchromosomal insertion of ins(1;8)(p22.1;q22q23)Chih-Ping Chen, Chao-Yun Wu, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 12, 2021
Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening resultChih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 15, 2017
Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defectChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|December 16, 2017
Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesisChih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 25, 2023
Concomitance of 47,XXY, a balanced reciprocal translocation of t(4;17)(q12;q11.2) encompassing SPINK2 at 4q12 and NOS at 17q11.2 and an AZFa sY86 deletion in an infertile maleFang-Tzu Wu, Chih-Ping Chen, Shin-Wen Chen, et al.
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