A Clinical Service to Support the Return of Secondary Genomic Findings in Human Research

Human genome and exome sequencing are powerful research tools that can generate secondary findings beyond the scope of the research. Most secondary genomic findings are of low importance, but some (for a current estimate of 1%–3% of individuals) confer high risk of a serious disease that could be mi...

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書誌詳細
出版年:Am J Hum Genet
主要な著者: Darnell, Andrew J., Austin, Howard, Bluemke, David A., Cannon, Richard O., Fischbeck, Kenneth, Gahl, William, Goldman, David, Grady, Christine, Greene, Mark H., Holland, Steven M., Hull, Sara Chandros, Porter, Forbes D., Resnik, David, Rubinstein, Wendy S., Biesecker, Leslie G.
フォーマット: Artigo
言語:Inglês
出版事項: Elsevier 2016
主題:
Commentary
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4800041/
https://ncbi.nlm.nih.gov/pubmed/26942283
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2016.01.010
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