公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2014 | A case of severe factor XIII deficiency with unusual uniparental disomy heredity | Lin, Ching-Yeh; Chen, Ming; Chang, Shun-Ping; Lin, Bo-Do; Ho, Wan-Ling; Lin, Jen-Shiou; Kuo, Su-Fong; Lin, Kai-Sin; 林凱信 | Haemophilia | | | |
2009 | A Case of Restrictive Dermopathy with Complete Chorioamniotic Membrane Separation Caused by a Novel Homozygous Nonsense Mutation in the Zmpste24 Gene | 陳明; 馬國欽; 柯瑜媛; 張舜評; 陳持平; 李東杰; 李孟倫; 李美慧; 陳子和; 陳加祥; 林惠美; 劉青山; CHEN, MING; MA, GWO-CHIN; KE, YU-YUAN; CHANG, SHUN-PING; CHEN, CHIH-PING; LEE, DONG-JAY; LEE, MENG-LUEN; LEE, MEI-HUI; CHEN, TZE-HO; CHEN, CHIA-HSIANG; LIN, HUI-MEI; LIU, CHIN-SAN | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | | | |
2009 | Differential Expression of NUDT9 at Different Phases of The Menstrual Cycle and in Different Components of Normal and Neoplastic Human Endometrium | MING CHEN ; CHEN, LING-YUN; CHEN, TZE-HO; WEN, PAO- YING; CHOU, CHIA-HUNG; YING, TSUNG-HO; CHANG, SHUN-PING; MA, GWO-CHIN; CHEN, MING | Taiwanese Journal of Obstetrics and Gynecology | 3 | 3 | |
2006 | A novel heterozygous missense mutation 377T > C (V126A) of TGIF gene in a family segregated with holoprosencephaly and moyamoya disease | MING CHEN ; Kuo, Shou-Jen; Liu, Chin-San; Chen, Wei-Liang; TSANG-MING KO ; Chen, Tze-Ho; Chang, Shun-Ping; Huang, Chien-Hao; Chang, Yih-Yuan; Wang, Bao-Tyan | Prenatal diagnosis | 12 | 10 | |
2024 | De Novo Noninversion Variants Implicated in Sporadic Hemophilia A: A Variant Origin and Timing Study | Chen, Ming; MING-CHING SHEN ; Chang, Shun-Ping; Ma, Gwo-Chin; Lee, Dong-Jay; Yan, Adeline | International journal of molecular sciences | | | |
2022 | Origin and timing of de novo variants implicated in type 2 von Willebrand disease | MING CHEN; MING-CHING SHEN ; Chang, Shun-Ping; Ma, Gwo-Chin; Huang, Ying-Chih; Lin, Ching-Yeh | Journal of cellular and molecular medicine | 1 | 0 | |
2021 | Preimplantation genetic diagnosis in hereditary hearing impairment | HSIN-LIN CHEN ; PEI-HSUAN LIN ; Chiang Yu-ting; Huang, Wen-Jie; Lin, Chi-Fang; Ma, Gwo-Chin; Chang, Shun-Ping; Fan, Jun-Yang; SHIN-YU LIN ; Chen-Chi Wu ; MING CHEN | Diagnostics | 2 | 2 | |
2019 | Preimplantation Genetic Diagnosis of Neurodegenerative Diseases: Review of Methodologies and Report of Our Experience as a Regional Reference Laboratory | Liao, Chun-Hua; Chang, Ming-Yuh; Ma, Gwo-Chin; Chang, Shun-Ping; Lin, Chi-Fang; Lin, Wen-Hsiang; Chen, Hsin-Fu; SHEE-UAN CHEN ; Lee, Yi-Chung; CHI-CHAO CHAO ; MING CHEN; SUNG-TSANG HSIEH | Diagnostics (Basel, Switzerland) | 8 | 5 | |
2006 | Prenatal Identification of Small Supernumerary Marker Chromosomes by Fish in an Infant Born with Mild Congenital Anomalies | 于宏燦 ; CHEN, MING; CHANG, SHUN-PING; YIN, PAO-LUN; KUO, SHOU-JEN; YU, H-T; WANG, BAO- TYAN | Prenatal Diagnosis | | | |
2022 | Skewed X-Chromosome Inactivation and Parental Gonadal Mosaicism Are Implicated in X-Linked Recessive Female Hemophilia Patients | MING-CHING SHEN ; Chang, Shun-Ping; Lee, Dong-Jay; Lin, Wen-Hsiang; Chen, Ming; Ma, Gwo-Chin | Diagnostics (Basel, Switzerland) | 2 | 1 | |
2008 | The Spectrum of the Factor 8 (F8) Defects in Taiwanese Patients with Haemophilia A | MA, GWO-CHIN; CHANG, SHUN-PING; CHEN, MING; KUO, SHOU-JEN; CHANG, CHENG-SHYONG; SHEN, MING-CHING | HAEMOPHILIA | | | |