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Cancer Genetics and Cytogenetics|August 5, 2010
Number of somatic mutations in the mitochondrial D-loop region indicates poor prognosis in breast cancer, independent of TP53 mutationShou-Jen Kuo, Ming Chen, Gwo-Chin Ma, et al.
Prenatal Diagnosis|February 14, 2006
A novel heterozygous missense mutation 377T > C (V126A) of TGIF gene in a family segregated with holoprosencephaly and moyamoya diseaseMing Chen, Shou-Jen Kuo, Chin-San Liu, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 10, 2025
Utility of long-read sequencing to delineate a rare large deletion of beta-globin gene which escaped Sanger sequencing at prenatal diagnosis in a family clustered with hereditary persistence of fetal hemoglobinDong-Jay Lee, Shun-Ping Chang, Min-Jun Liao, et al.
Prenatal Diagnosis|November 1, 2008
A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapyGwo-Chin Ma, Chin-San Liu, Shun-Ping Chang, 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|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|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|January 4, 2012
Preimplantation and prenatal genetic diagnosis of aromatic L-amino acid decarboxylase deficiency with an amplification refractory mutation system-quantitative polymerase chain reactionShou-Jen Kuo, Gwo-Chin Ma, Shun-Ping Chang, et al.
Diagnostics (Basel, Switzerland)|December 24, 2021
Preimplantation Genetic Diagnosis in Hereditary Hearing ImpairmentHsin-Lin Chen, Pei-Hsuan Lin, Yu-Ting Chiang, et al.
Molecular Cytogenetics|July 10, 2015
Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verificationYu-Shih Yang, Shun-Ping Chang, Hsin-Fu Chen, et al.
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