Gwo-Chin Ma - Search Results

Year	Number of Results
2007	2
2008	2
2009	2
2010	6
2011	6
2012	5
2013	3
2014	1
2015	1
2016	4
2017	2
2018	2
2019	4
2020	3
2021	6
2022	4

1

Preimplantation genetic diagnosis and screening: Current status and future challenges.

Chen HF, Chen SU, Ma GC, Hsieh ST, Tsai HD, Yang YS, Chen M. Chen HF, et al. Among authors: ma gc. J Formos Med Assoc. 2018 Feb;117(2):94-100. doi: 10.1016/j.jfma.2017.08.006. Epub 2017 Sep 6. J Formos Med Assoc. 2018. PMID: 28888353 Free article. Review.

2

Preimplantation Genetic Diagnosis in Hereditary Hearing Impairment.

Chen HL, Lin PH, Chiang YT, Huang WJ, Lin CF, Ma GC, Chang SP, Fan JY, Lin SY, Wu CC, Chen M. Chen HL, et al. Among authors: ma gc. Diagnostics (Basel). 2021 Dec 20;11(12):2395. doi: 10.3390/diagnostics11122395. Diagnostics (Basel). 2021. PMID: 34943631 Free PMC article.

3

Preimplantation genetic diagnosis of hemophilia A.

Chen M, Chang SP, Ma GC, Lin WH, Chen HF, Chen SU, Tsai HD, Tsai FP, Shen MC. Chen M, et al. Among authors: ma gc. Thromb J. 2016 Oct 4;14(Suppl 1):33. doi: 10.1186/s12959-016-0098-9. eCollection 2016. Thromb J. 2016. PMID: 27766059 Free PMC article. Review.

4

Genotype and phenotype studies of Lowe syndrome in three families in Taiwan.

Chen KJ, Wu HR, Chao MC, Chang TM, Chien JW, Chen M, Ma GC, Ke YY. Chen KJ, et al. Among authors: ma gc. Pediatr Neonatol. 2021 May;62(3):327-328. doi: 10.1016/j.pedneo.2021.01.012. Epub 2021 Feb 6. Pediatr Neonatol. 2021. PMID: 33745830 Free article. No abstract available.

5

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

Huang TX, Ma GC, Chen M, Li WF, Shaw SW. Huang TX, et al. Among authors: ma gc. Front Genet. 2021 Dec 14;12:612100. doi: 10.3389/fgene.2021.612100. eCollection 2021. Front Genet. 2021. PMID: 34970295 Free PMC article.

6

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

Chang TY, Chen SW, Lin WH, Huang CE, Evans MI, Chung IF, Wu JW, Ma GC, Chen M. Chang TY, et al. Among authors: ma gc. Diagnostics (Basel). 2021 Jun 16;11(6):1102. doi: 10.3390/diagnostics11061102. Diagnostics (Basel). 2021. PMID: 34208639 Free PMC article.

7

Low-level mosaicism for trisomy 16 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome.

Chen CP, Chen M, Wang LK, Chern SR, Wu PS, Ma GC, Chang SP, Chen SW, Wu FT, Lee CC, Chen YY, Wang W. Chen CP, et al. Among authors: ma gc. Taiwan J Obstet Gynecol. 2021 Mar;60(2):345-349. doi: 10.1016/j.tjog.2021.01.014. Taiwan J Obstet Gynecol. 2021. PMID: 33678340 Free article.

8

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

Yao TY, Wu WJ, Law KS, Lee MH, Chang SP, Lee DJ, Lin WH, Chen M, Ma GC. Yao TY, et al. Among authors: ma gc. Diagnostics (Basel). 2021 Aug 12;11(8):1457. doi: 10.3390/diagnostics11081457. Diagnostics (Basel). 2021. PMID: 34441391 Free PMC article.

9

Prenatal diagnosis of partial monosomy 21q (21q22.1→qter) associated with intrauterine growth restriction and corpus callosum dysgenesis.

Chen YC, Wu WJ, Chang SP, Ma GC, Chen M. Chen YC, et al. Among authors: ma gc. Taiwan J Obstet Gynecol. 2020 Jan;59(1):157-161. doi: 10.1016/j.tjog.2019.11.027. Taiwan J Obstet Gynecol. 2020. PMID: 32039787 Free article.

10

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 Fetal Skeletal Dysplasia during Prenatal Ultrasound.

Chang TY, Chung IF, Wu WJ, Chang SP, Lin WH, Ginsberg NA, Ma GC, Chen M. Chang TY, et al. Among authors: ma gc. Diagnostics (Basel). 2020 May 7;10(5):286. doi: 10.3390/diagnostics10050286. Diagnostics (Basel). 2020. PMID: 32392875 Free PMC article.

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