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Curated incidence of lysosomal storage diseases from the Taiwan Biobank.
NPJ Genom Med. 2023 Sep 23;8(1):27. doi: 10.1038/s41525-023-00372-x.
NPJ Genom Med. 2023.
PMID: 37741878
Free PMC article.
Frequency and spectrum of actionable pathogenic secondary findings in Taiwanese exomes.
Kuo CW, Hwu WL, Chien YH, Hsu C, Hung MZ, Lin IL, Lai F, Lee NC.
Kuo CW, et al. Among authors: hung mz.
Mol Genet Genomic Med. 2020 Oct;8(10):e1455. doi: 10.1002/mgg3.1455. Epub 2020 Aug 14.
Mol Genet Genomic Med. 2020.
PMID: 32794656
Free PMC article.
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Comparison of GATK and DeepVariant by trio sequencing.
Lin YL, Chang PC, Hsu C, Hung MZ, Chien YH, Hwu WL, Lai F, Lee NC.
Lin YL, et al. Among authors: hung mz.
Sci Rep. 2022 Feb 2;12(1):1809. doi: 10.1038/s41598-022-05833-4.
Sci Rep. 2022.
PMID: 35110657
Free PMC article.
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Utility of whole-exome sequencing for patients with multiple congenital anomalies with or without intellectual disability/developmental delay in East Asia population.
Hsu RH, Lee CH, Chien YH, Lin SP, Hung MZ, Chen NC, Lin YL, Hwu WL, Lee NC.
Hsu RH, et al. Among authors: hung mz.
Mol Genet Genomic Med. 2023 Jun;11(6):e2160. doi: 10.1002/mgg3.2160. Epub 2023 Feb 27.
Mol Genet Genomic Med. 2023.
PMID: 36849876
Free PMC article.
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Ethnically unique disease burden and limitations of current expanded carrier screening panels.
Chen CL, Lee NC, Chien YH, Hwu WL, Hung MZ, Lin YL, Lin SY, Lee CN.
Chen CL, et al. Among authors: hung mz.
Int J Gynaecol Obstet. 2024 Mar;164(3):918-924. doi: 10.1002/ijgo.15072. Epub 2023 Sep 8.
Int J Gynaecol Obstet. 2024.
PMID: 37681470
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DYNC1H1 variant associated with epilepsy: Expanding the phenotypic spectrum.
Chung CT, Lee NC, Fan SP, Hung MZ, Lin YH, Chen CH, Jao T.
Chung CT, et al. Among authors: hung mz.
Epilepsy Behav Rep. 2022 Dec 28;21:100580. doi: 10.1016/j.ebr.2022.100580. eCollection 2023.
Epilepsy Behav Rep. 2022.
PMID: 36636459
Free PMC article.
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