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Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers.
Walker LC, Marquart L, Pearson JF, Wiggins GA, O'Mara TA, Parsons MT; BCFR; Barrowdale D, McGuffog L, Dennis J, Benitez J, Slavin TP, Radice P, Frost D; EMBRACE; Godwin AK, Meindl A, Schmutzler RK; GEMO Study Collaborators; Isaacs C, Peshkin BN, Caldes T, Hogervorst FB; HEBON; Lazaro C, Jakubowska A, Montagna M; KConFab Investigators; Chen X, Offit K, Hulick PJ, Andrulis IL, Lindblom A, Nussbaum RL, Nathanson KL, Chenevix-Trench G, Antoniou AC, Couch FJ, Spurdle AB. Walker LC, et al. Among authors: lindblom a. Eur J Hum Genet. 2017 Apr;25(4):432-438. doi: 10.1038/ejhg.2016.203. Epub 2017 Feb 1. Eur J Hum Genet. 2017. PMID: 28145423 Free PMC article.
BRCA2 germline mutations in Swedish breast cancer families.
Chen J, Hedman MZ, Arver BW, Sigurdsson S, Eyfjörd JE, Lindblom A. Chen J, et al. Among authors: lindblom a. Eur J Hum Genet. 1998 Mar-Apr;6(2):134-9. doi: 10.1038/sj.ejhg.5200167. Eur J Hum Genet. 1998. PMID: 9781057
Hereditary breast cancer: a review.
Arver B, Du Q, Chen J, Luo L, Lindblom A. Arver B, et al. Among authors: lindblom a. Semin Cancer Biol. 2000 Aug;10(4):271-88. doi: 10.1006/scbi.2000.0325. Semin Cancer Biol. 2000. PMID: 10966850 Review.
528 results