English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12145/12927 (94%)
Visitors : 936081      Online Users : 604
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
    •  Adv. Search
    Home ‧ Login ‧ Upload ‧ Help ‧ About ‧ Administer Goto mobile version

    Category

    Loading community tree, please wait....

    Year

    Loading year class tree, please wait....

    Items for Author "Weng, HY" 

    Return to Browse by Author

    Showing 12 items.

    Collection Date Title Relation Bitstream
    [其他] 會議論文/會議摘要 2019-07 Identify the predisposition genes to endometrial cancer -
    [其他] 期刊論文 2019-07 Elucidating unique axonal dysfunction between nitrous oxide abuse and vitamin B12 deficiency -
    [蔡世峯] 期刊論文 2023-06 Outbreak investigation in a COVID-19 designated hospital: The combination of phylogenetic analysis and field epidemiology study suggesting airborne transmission -
    [蔡世峯] 期刊論文 2023 Emergence and persistent dominance of SARS-CoV-2 omicron BA.2.3.7 variant, Taiwan -
    [蔡世峯] 期刊論文 2022-12 Genomic profiling with whole-exome sequencing revealed distinct mutations and novel pathways in Asian melanoma -
    [蔡世峯] 期刊論文 2022-10 Protein O-fucosyltransferase-1 mutation in familial Dowling-Degos Disease concomitant with atopic dermatitis -
    [蔡世峯] 期刊論文 2022-08-17 Disclosing an in-frame deletion of the titin gene as the possible predisposing factor of anthracycline-induced cardiomyopathy: A case report -
    [蔡世峯] 期刊論文 2022-01 Novel ADAR1 mutations in three cases of psoriasis coexisting with dyschromatosis symmetrica hereditaria -
    [蔡世峯] 期刊論文 2020-12 Diagnosis of Arboleda-Tham syndrome by whole genome sequencing in an Asian boy with severe developmental delay -
    [蔡世峯] 期刊論文 2019-08-20 A novel BTK gene mutation in a child with atypical X-linked agammaglobulinemia and recurrent hemophagocytosis: A case report -
    [蔡世峯] 期刊論文 2017-09 Novel mutations of the tetratricopeptide repeat domain 7A gene and phenotype/genotype comparison -
    [蔡世峯] 期刊論文 2010-01 Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis -

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback