首页> PloS one> Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.

Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles.

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第一作者： Francisco Javier,Gracia-Aznarez

第一单位： Human Genetics Group, Spanish National Cancer Centre (CNIO), Madrid, Spain.

作者： Francisco Javier,Gracia-Aznarez ^[1] ; Victoria,Fernandez ; Guillermo,Pita ; Paolo,Peterlongo ; Orlando,Dominguez ; Miguel,de la Hoya ; Mercedes,Duran ; Ana,Osorio ; Leticia,Moreno ; Anna,Gonzalez-Neira ; Juan Manuel,Rosa-Rosa ; Olga,Sinilnikova ; Sylvie,Mazoyer ; John,Hopper ; Conchi,Lazaro ; Melissa,Southey ; Fabrice,Odefrey ; Siranoush,Manoukian ; Irene,Catucci ; Trinidad,Caldes ; Henry T,Lynch ; Florentine S M,Hilbers ; Christi J,van Asperen ; Hans F A,Vasen ; David,Goldgar ; Paolo,Radice ; Peter,Devilee ; Javier,Benitez

作者单位： Human Genetics Group, Spanish National Cancer Centre (CNIO), Madrid, Spain. ^[1]

医学主题词等位基因(Alleles);乳腺肿瘤(Breast Neoplasms);女(雌)性(Female);基因, BRCA1(Genes, BRCA1);基因, BRCA2(Genes, BRCA2);人类(Humans)

DOI 10.1371/journal.pone.0055681

PMID 23409019

发布时间 2022-03-10

基金项目

U01 CA069417/CA/NCI NIH HHS/United States U01 CA069638/CA/NCI NIH HHS/United States U01 CA69417/CA/NCI NIH HHS/United States U01 CA069467/CA/NCI NIH HHS/United States U01 CA069398/CA/NCI NIH HHS/United States U01 CA69638/CA/NCI NIH HHS/United States CA-06-503/CA/NCI NIH HHS/United States U01 CA069446/CA/NCI NIH HHS/United States U01 CA69467/CA/NCI NIH HHS/United States U01 CA069631/CA/NCI NIH HHS/United States U01 CA69398/CA/NCI NIH HHS/United States UL 2009-4388/PHS HHS/United States U01 CA69446/CA/NCI NIH HHS/United States U01 CA69631/CA/NCI NIH HHS/United States

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