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Diagnostics (Basel, Switzerland)|May 13, 2020
Whole Exome Sequencing with Comprehensive Gene Set Analysis Identified a Biparental-Origin Homozygous c.509G>A Mutation in <i>PPIB</i> Gene Clustered in Two Taiwanese Families Exhibiting Fetal Skeletal Dysplasia during Prenatal UltrasoundTing-Yu Chang, I-Fang Chung, Wan-Ju Wu, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 4, 2009
Differential expression of NUDT9 at different phases of the menstrual cycle and in different components of normal and neoplastic human endometriumLing-Yun Chen, Tze-Ho Chen, Pao-Ying Wen, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 30, 2026
Hidden translocation between 15qter and 18qter impressed during cycles of preimplantation genetic testing using linkage analyses and chromosome microarray subsequently verified by fluorescence in situ hybridizationGwo-Chin Ma, Chi-Fang Lin, Wen-Hsiang 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.
Diagnostics (Basel, Switzerland)|August 27, 2021
Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome MicroarrayTien-Yu Yao, Wan-Ju Wu, Kim-Seng Law, et al.
Thrombosis Journal|October 22, 2016
Preimplantation genetic diagnosis of hemophilia AMing Chen, Shun-Ping Chang, Gwo-Chin Ma, et al.
Taiwanese Journal of Obstetrics & Gynecology|June 11, 2017
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11Chih-Ping Chen, Ming Chen, Pu-Tsui Wang, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 5, 2023
Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive NIPT result suspicious of trisomy 13, a CVS result of mosaic trisomy 13, cytogenetic discrepancy in various tissues and a favorable fetal outcomeChih-Ping Chen, Ming Chen, Gwo-Chin Ma, et al.
International Journal of Molecular Sciences|March 14, 2026
Genotype-Specific Postural Control Deficits in Hemophilia A: Insights from Center of Pressure Analysis Beyond Radiographic ArthropathyYa-Chi Huang, Wei-Long Wang, Hsuan-Yu Lin, et al.
Gene|December 31, 2013
Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistryChih-Ping Chen, Ming Chen, Chen-Yu Chen, et al.
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