Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Fanconi Anemia and XRCC2[original query] |
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Rare mutations in XRCC2 increase the risk of breast cancer. American journal of human genetics 2012 Apr 90 (4): 734-9. Park D J, Lesueur F, Nguyen-Dumont T, Pertesi M, Odefrey F, Hammet F, Neuhausen S L, John E M, Andrulis I L, Terry M B, Daly M, Buys S, Le Calvez-Kelm F, Lonie A, Pope B J, Tsimiklis H, Voegele C, Hilbers F M, Hoogerbrugge N, Barroso A, Osorio A, , , Giles G G, Devilee P, Benitez J, Hopper J L, Tavtigian S V, Goldgar D E, Southey M |
Frequency of heterozygous germline pathogenic variants in genes for Fanconi anemia in patients with non-BRCA1/BRCA2 breast cancer: a meta-analysis. Breast cancer research and treatment 2020 Jun . Alter Blanche P, Best Ana |
FANCL gene mutations in premature ovarian insufficiency. Human mutation 2020 Feb . Yang Yajuan, Guo Ting, Liu Ran, Ke Hanni, Xu Weiwei, Zhao Shidou, Qin Yingyi |
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- Page last updated:Jun 02, 2023
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