Relevance of Copy Number Variation at Chromosome X in Male Fetuses Inherited from the Mother May Be Ascertained by Including Male Relatives from the Maternal Lineage in Addition to...

por Chen, Ming, Wu, Wan-Ju, Lee, Mei-Hui, Ku, Tien-Hsiung, Ma, Gwo-Chin
Publicado 2020

Difficulties of Prenatal Genetic Counseling for a Subsequent Child in a Family With Multiple Genetic Variations

por Huang, Ting-Xuan, Ma, Gwo-Chin, Chen, Ming, Li, Wen-Fang, Shaw, Steven W.
Publicado 2021

Proposal for Practical Approach in Prenatal Diagnosis of Beckwith–Wiedemann Syndrome and Review of the Literature

por Ma, Gwo-Chin, Chen, Tze-Ho, Wu, Wan-Ju, Lee, Dong-Jay, Lin, Wen-Hsiang, Chen, Ming
Publicado 2022

Skewed X-Chromosome Inactivation and Parental Gonadal Mosaicism Are Implicated in X-Linked Recessive Female Hemophilia Patients

por Shen, Ming-Ching, Chang, Shun-Ping, Lee, Dong-Jay, Lin, Wen-Hsiang, Chen, Ming, Ma, Gwo-Chin
Publicado 2022

Origin and timing of de novo variants implicated in type 2 von Willebrand disease

por Chen, Ming, Shen, Ming‐Ching, Chang, Shun‐Ping, Ma, Gwo‐Chin, Huang, Ying‐Chih, Lin, Ching‐Yeh
Publicado 2022

De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD

por Shen, Ming-Ching, Chen, Ming, Ma, Gwo-Chin, Chang, Shun-Ping, Lin, Ching-Yeh, Lin, Bo-Do, Hsieh, Han-Ni
Publicado 2016

Prenatal Diagnosis of Autosomal Recessive Renal Tubular Dysgenesis with Anhydramnios Caused by a Mutation in the AGT Gene

por Ma, Gwo-Chin, Chen, Ying-Chung, Wu, Wan-Ju, Chang, Shun-Ping, Chang, Ting-Yu, Lin, Wen-Hsiang, Chen, Ming
Publicado 2019

A pilot proof-of-principle study to compare fresh and vitrified cycle preimplantation genetic screening by chromosome microarray and next generation sequencing

por Ma, Gwo-Chin, Chen, Hsin-Fu, Yang, Yu-Shih, Lin, Wen-Hsiang, Tsai, Feng-Po, Lin, Chi-Fang, Chiu, Chi, Chen, Ming
Publicado 2016

Genome-Wide Microarray Analysis Suggests Transcriptomic Response May Not Play a Major Role in High- to Low-Altitude Acclimation in Harvest Mouse (Micromys minutus)

por Chen, Tze-Ho, Ma, Gwo-Chin, Lin, Wen-Hsiang, Lee, Dong-Jay, Wu, Sheng-Hai, Liao, Ben-Yang, Chen, Ming, Lin, Liang-Kong
Publicado 2019

Whole Exome Sequencing with Comprehensive Gene Set Analysis Identified a Biparental-Origin Homozygous c.509G>A Mutation in PPIB Gene Clustered in Two Taiwanese Families Exhibiting...

por Chang, Ting-Yu, Chung, I-Fang, Wu, Wan-Ju, Chang, Shun-Ping, Lin, Wen-Hsiang, Ginsberg, Norman A., Ma, Gwo-Chin, Chen, Ming
Publicado 2020

Preimplantation genetic diagnosis of hemophilia A

por Chen, Ming, Chang, Shun-Ping, Ma, Gwo-Chin, Lin, Wen-Hsian, Chen, Hsin-Fu, Chen, Shee-Uan, Tsai, Horng-Der, Tsai, Feng-Po, Shen, Ming-Ching
Publicado 2016

Low-molecular-weight-heparin can benefit women with recurrent pregnancy loss and sole protein S deficiency: a historical control cohort study from Taiwan

por Shen, Ming-Ching, Wu, Wan-Ju, Cheng, Po-Jen, Ma, Gwo-Chin, Li, Wen-Chu, Liou, Jui-Der, Chang, Cheng-Shyong, Lin, Wen-Hsiang, Chen, Ming
Publicado 2016

Comparison of Genetic Profiling between Primary Tumor and Circulating Tumor Cells Captured by Microfluidics in Epithelial Ovarian Cancer: Tumor Heterogeneity or Allele Dropout?

por Chang, Ting-Yu, Chen, Sheng-Wen, Lin, Wen-Hsiang, Huang, Chung-Er, Evans, Mark I., Chung, I-Fang, Wu, Janne-Wha, Ma, Gwo-Chin, Chen, Ming
Publicado 2021

Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Mic...

por Yao, Tien-Yu, Wu, Wan-Ju, Law, Kim-Seng, Lee, Mei-Hui, Chang, Shun-Ping, Lee, Dong-Jay, Lin, Wen-Hsiang, Chen, Ming, Ma, Gwo-Chin
Publicado 2021

A Silicon-based Coral-like Nanostructured Microfluidics to Isolate Rare Cells in Human Circulation: Validation by SK-BR-3 Cancer Cell Line and Its Utility in Circulating Fetal Nucl...

por Ma, Gwo-Chin, Lin, Wen-Hsiang, Huang, Chung-Er, Chang, Ting-Yu, Liu, Jia-Yun, Yang, Ya-Jun, Lee, Mei-Hui, Wu, Wan-Ju, Chang, Yun-Shiang, Chen, Ming
Publicado 2019

Noninvasive prenatal diagnosis of fetal aneuploidy by circulating fetal nucleated red blood cells and extravillous trophoblasts using silicon-based nanostructured microfluidics

por Huang, Chung-Er, Ma, Gwo-Chin, Jou, Hei-Jen, Lin, Wen-Hsiang, Lee, Dong-Jay, Lin, Yi-Shing, Ginsberg, Norman A., Chen, Hsin-Fu, Chang, Frank Mau-Chung, Chen, Ming
Publicado 2017

Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification

por Yang, Yu-Shih, Chang, Shun-Ping, Chen, Hsin-Fu, Ma, Gwo-Chin, Lin, Wen-Hsiang, Lin, Chi-Fang, Tsai, Feng-Po, Wu, Cheng-Hsuan, Tsai, Horng-Der, Lee, Tsung-Hsien, Chen, Ming
Publicado 2015

Preimplantation Genetic Diagnosis in Hereditary Hearing Impairment

por Chen, Hsin-Lin, Lin, Pei-Hsuan, Chiang, Yu-Ting, Huang, Wen-Jie, Lin, Chi-Fang, Ma, Gwo-Chin, Chang, Shun-Ping, Fan, Jun-Yang, Lin, Shin-Yu, Wu, Chen-Chi, Chen, Ming
Publicado 2021

Preimplantation Genetic Diagnosis of Neurodegenerative Diseases: Review of Methodologies and Report of Our Experience as a Regional Reference Laboratory

por Liao, Chun-Hua, Chang, Ming-Yuh, Ma, Gwo-Chin, Chang, Shun-Ping, Lin, Chi-Fang, Lin, Wen-Hsiang, Chen, Hsin-Fu, Chen, Shee-Uan, Lee, Yi-Chung, Chao, Chi-Chao, Chen, Ming, Hsieh, Sung-Tsang
Publicado 2019

Fosmid library end sequencing reveals a rarely known genome structure of marine shrimp Penaeus monodon

por Huang, Shiao-Wei, Lin, You-Yu, You, En-Min, Liu, Tze-Tze, Shu, Hung-Yu, Wu, Keh-Ming, Tsai, Shih-Feng, Lo, Chu-Fang, Kou, Guang-Hsiung, Ma, Gwo-Chin, Chen, Ming, Wu, Dongying, Aoki, Takashi, Hirono, Ikuo, Yu, Hon-Tsen
Publicado 2011