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Table representation of search results timeline featuring number of search results per year.

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
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49 results
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Page 1
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.
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.
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.
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.
49 results