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Harmonizing the interpretation of genetic variants across the world: the Malaysian experience

BACKGROUND: Databases for gene variants are very useful for sharing genetic data and to facilitate the understanding of the genetic basis of diseases. This report summarises the issues surrounding the development of the Malaysian Human Variome Project Country Node. The focus is on human germline var...

詳細記述

保存先:
書誌詳細
出版年:BMC Res Notes
主要な著者: Nik Hassan, Nik Norliza, Plazzer, John-Paul, Smith, Timothy D., Halim-Fikri, Hashim, Macrae, Finlay, Zubaidi AL, A., Zilfalil, Bin Alwi
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2016
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4768322/
https://ncbi.nlm.nih.gov/pubmed/26915360
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-015-1798-0
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