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Taiwanese Journal of Obstetrics & Gynecology|May 18, 2020
Perinatal cytogenetic discrepancy in a fetus with low-level mosaicism for trisomy 21 and a favorable outcomeChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 2, 2017
Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormalityChih-Ping Chen, Chung-Hu Fu, Yi-Hui Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 10, 2022
Detection of mosaicism for 46,X,i(Y) (q10) in the blood lymphocytes in a phenotypically normal male neonate with prenatally detected 45,X/46, XY at amniocentesis and cytogenetic discrepancy in various tissuesChih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 30, 2016
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)Chih-Ping Chen, Fung-Yu Hung, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 25, 2022
Prenatal diagnosis and molecular cytogenetic characterization of a de novo deletion of 4q34.1→qter associated with low PAPP-A and low PlGF in the first-trimester maternal serum screening, congenital heart defect on fetal ultrasound and a false negative non-invasive prenatal testing (NIPT) resultChih-Ping Chen, Shin-Wen Chen, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 5, 2020
Prenatal diagnosis of mosaicism for trisomy 11 in a single colony at amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen, Shun-Long Weng, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 18, 2017
Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicismChih-Ping Chen, Chris Tsai, Ming-Huei Lin, et al.
Taiwanese Journal of Obstetrics & Gynecology|February 19, 2022
Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10)Chih-Ping Chen, Ming Chen, Gwo-Chin Ma, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 4, 2016
Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegalyChih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 30, 2016
Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of FallotChih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, et al.
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