Screening RAD51C nucleotide alterations in patients with a family history of breast and ovarian cancer
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology
Link
http://link.springer.com/content/pdf/10.1007/s10549-010-1095-5.pdf
Reference19 articles.
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4. Xia B, Dorsman JC, Ameziane N, de Vries Y, Rooimans MA, Sheng Q, Pals G, Errami A, Gluckman E, Llera J, Wang W, Livingston DM, Joenje H, de Winter JP (2007) Fanconi anemia is associated with a defect in the brca2 partner palb2. Nat Genet 39(2):159–161. doi: 10.1038/ng1942
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1. Molecular Genetic Characteristics of FANCI, a Proposed New Ovarian Cancer Predisposing Gene;Genes;2023-01-20
2. A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene;Genome Medicine;2021-12
3. Exome Sequencing in BRCA1-2 Candidate Familias: The Contribution of Other Cancer Susceptibility Genes;Frontiers in Oncology;2021-05-07
4. The genetic analysis of a founder Northern American population of European descent identifies FANCI as a candidate familial ovarian cancer risk gene;2020-05-08
5. BRIP1, RAD51C, and RAD51D mutations are associated with high susceptibility to ovarian cancer: mutation prevalence and precise risk estimates based on a pooled analysis of ~30,000 cases;Journal of Ovarian Research;2020-05-02
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