公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
2014 | Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization | MING CHEN ; YU-SHIH YANG ; JIN-CHUNG SHIH ; Lin W.-H.; Lee D.-J.; Lin Y.-S.; Chou C.-H.; Cameron A.D.; Ginsberg N.A.; CHI-AN CHEN ; Lee M.-L.; Ma G.-C. | Ultrasound in Obstetrics and Gynecology | 20 | 21 | |
2010 | Mirror-image type D interrupted aortic arch: A novel cardiac phenotype providing some perspective in the del22q11.2 syndrome | Lee M.-L.; MING CHEN ; Yang A.D.; ING-SH CHIU | International Journal of Cardiology | 2 | 1 | |
2017 | Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions | MING CHEN | Taiwanese Journal of Obstetrics and Gynecology | 0 | 0 | |
2013 | Mosaic small supernumerary marker chromosome 1 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review | MING CHEN | Gene | 1 | 1 | |
2011 | Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses | MING CHEN | Genetic Counseling | | | |
2007 | Mutation analysis of TSC gene in tuberous sclerosis complex patient - Case report | MING CHEN | Dermatologica Sinica | | | |
2017 | Noninvasive prenatal diagnosis of fetal aneuploidy by circulating fetal nucleated red blood cells and extravillous trophoblasts using silicon-based nanostructured microfluidics | Huang, Chung-Er; Ma, Gwo-Chin; Jou, Hei-Jen; Lin, Wen-Hsiang; Lee, Dong-Jay; Lin, Yi-Shing; Ginsberg, Norman A; HSIN-FU CHEN ; Chang, Frank Mau-Chung; MING CHEN | Molecular cytogenetics | 36 | 32 | |
2014 | Noninvasive prenatal testing for whole fetal chromosomal aneuploidies: A multicenter prospective cohort trial in Taiwan | MING CHEN | Fetal Diagnosis and Therapy | 23 | 22 | |
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 | |
2016 | De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD | MING-CHING SHEN ; MING CHEN ; Ma G.-C.; Chang S.-P.; Lin C.-Y.; Lin B.-D.; Hsieh H.-N. | Thrombosis Journal | 6 | 0 | |
2010 | Number of somatic mutations in the mitochondrial D-loop region indicates poor prognosis in breast cancer, independent of TP53 mutation | MING CHEN | Cancer Genetics and Cytogenetics | 20 | 19 | |
2009 | Outcomes in neonates with pulmonary atresia and intact ventricular septum underwent pulmonary valvulotomy and valvuloplasty using a flexible 2-french radiofrequency catheter | Lee M.-L.; Tsao L.-Y.; Chiu H.-Y.; MING CHEN ; ING-SH CHIU | Yonsei Medical Journal | 8 | 5 | |
2014 | Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells | MING CHEN | Taiwanese Journal of Obstetrics and Gynecology | 2 | 1 | |
2006 | Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3→q31.3) associated with Gorlin syndrome | MING CHEN | Prenatal Diagnosis | 25 | 23 | |
2006 | Persistent fifth aortic arch associated with 22q11.2 deletion syndrome | Lee M.-L.; Chen H.-N.; MING CHEN ; Tsao L.-Y.; Wang B.-T.; Lee M.-H.; ING-SH CHIU | Journal of the Formosan Medical Association | 12 | 12 | |
2008 | Phenotype and Genotype of Two Taiwanese Cystic Fibrosis Siblings and a Survey of Delta F508 in East Asians | MING CHEN | Pediatrics and Neonatology | 7 | 0 | |
2016 | A pilot proof-of-principle study to compare fresh and vitrified cycle preimplantation genetic screening by chromosome microarray and next generation sequencing | Ma, Gwo-Chin; MING CHEN ; HSIN-FU CHEN ; YU-SHIH YANG ; Lin, Wen-Hsiang; Tsai, Feng-Po; Lin, Chi-Fang; Chiu, Chi | Molecular Cytogenetics | 14 | 12 | |
2018 | Preimplantation genetic diagnosis and screening: Current status and future challenges | HSIN-FU CHEN ; SHEE-UAN CHEN ; Ma G.-C.; SUNG-TSANG HSIEH ; Tsai H.-D.; YU-SHIH YANG ; MING CHEN | Journal of the Formosan Medical Association | 35 | 33 | |
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 | |
2015 | Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: Validation and verification | YU-SHIH YANG ; Chang S.-P; HSIN-FU CHEN ; Ma G.-C; Lin W.-H; Lin C.-F; Tsai F.-P; Wu C.-H; Tsai H.-D; Lee T.-H; MING CHEN | Molecular Cytogenetics | 8 | 8 | |