ロード中...

BRCA1/2 Sequence Variants of Uncertain Significance: A Primer for Providers to Assist in Discussions and in Medical Management

INTRODUCTION. DNA variants of uncertain significance (VUS) are common outcomes of clinical genetic testing for susceptibility to cancer. A statistically rigorous model that provides a pathogenicity score for each variant has been developed to aid in the clinical management of patients undergoing gen...

詳細記述

保存先:
書誌詳細
主要な著者: Lindor, Noralane M., Goldgar, David E., Tavtigian, Sean V., Plon, Sharon E., Couch, Fergus J.
フォーマット: Artigo
言語:Inglês
出版事項: AlphaMed Press 2013
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3662842/
https://ncbi.nlm.nih.gov/pubmed/23615697
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1634/theoncologist.2012-0452
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!