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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 28, 2023. (Total: 223416Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Fanconi Anemia and XRCC2[original query]
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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