Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients-Reference-Cited by-同舟云学术

Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients

Published:2014-05-15 Issue:1 Volume:15 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Silva Felipe C,Lisboa Bianca CG,Figueiredo Marcia CP,Torrezan Giovana T,Santos Érika MM,Krepischi Ana C,Rossi Benedito M,Achatz Maria I,Carraro Dirce M

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/1471-2350-15-55.pdf

Reference41 articles.

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4. Ford D, Easton DF, Stratton M, Narod S, Goldgar D, Devilee P, Bishop DT, Weber B, Lenoir G, Chang-Claude J, Sobol H, Teare MD, Struewing J, Arason A, Scherneck S, Peto J, Rebbeck TR, Tonin P, Neuhausen S, Barkardottir R, Eyfjord J, Lynch H, Ponder BA, Gayther SA, Zelada-Hedman M, and the Breast Cancer Linkage Consortium: Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. the Breast Cancer Linkage Consortium. Am J Hum Genet. 1998, 62 (3): 676-689. 10.1086/301749.

5. Thorlacius S, Olafsdottir G, Tryggvadottir L, Neuhausen S, Jonasson JG, Tavtigian SV, Tulinius H, Ogmundsdottir HM, Eyfjörd JE: A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes. Nat Genet. 1996, 13 (1): 117-119. 10.1038/ng0596-117.

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