Showing results (121-130 of 151) with videos related to

Sort By:
Pageof 16
Taiwanese Journal of Obstetrics & Gynecology|December 16, 2017
Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1Chih-Ping Chen, Chih-Heng Hsieh, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 15, 2017
Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9Chih-Ping Chen, Ming Chen, Liang-Kai Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|August 15, 2017
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature reviewChih-Ping Chen, Ming Chen, Chia-Hsun Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|April 1, 2022
Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22Chih-Ping Chen, Ming Chen, Gwo-Chin Ma, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 12, 2020
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesisChih-Ping Chen, Te-Yao Hsu, Tsang-Ming Ko, et al.
Taiwanese Journal of Obstetrics & Gynecology|September 12, 2020
Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcomeChih-Ping Chen, Tsang-Ming Ko, Yi-Yung Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 19, 2021
Prenatal diagnosis of mosaic trisomy 16 by amniocentesis in a pregnancy associated with abnormal first-trimester screening result (low PAPP-A and low PlGF), intrauterine growth restriction and a favorable outcomeChih-Ping Chen, Fei-Hua Lan, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 8, 2021
Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytesChih-Ping Chen, Liang-Ming Lo, Tsang-Ming Ko, et al.
Taiwanese Journal of Obstetrics & Gynecology|December 16, 2017
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen, Tsang-Ming Ko, Yi-Yung Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 22, 2018
Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasoundChih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, et al.
Pageof 16