Mutational analysis ofBRCA1andBRCA2genes in Peruvian families with hereditary breast and ovarian cancer
Author:
Affiliation:
1. Centro de Genética y Biología Molecular; Facultad de Medicina Humana; Universidad de San Martín de Porres; Lima Perú
2. Unidad de Investigación Básica y Traslacional; Oncosalud-AUNA; Lima Perú
3. Unidad de la Mama; Oncosalud-AUNA; Lima Perú
Funder
Instituto Nacional de Salud, Origenetica, Oncosalud-AUNA, Universidad de San Martín de Porres
FINCyT
Publisher
Wiley
Subject
Genetics (clinical),Genetics,Molecular Biology
Reference62 articles.
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2. Prevalence of BRCA1 genomic rearrangements in a large cohort of Italian breast and breast/ovarian cancer families without detectable BRCA1 and BRCA2 point mutations;Agata;Genes Chromosom. Cancer,2006
3. The BRCA1 RING and BRCT domains cooperate in targeting BRCA1 to ionizing radiation-induced nuclear foci;Au;J. Biol. Chem.,2005
4. Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study;Borg;Hum. Mutat.,2010
5. Clinical considerations of BRCA1- and BRCA2-mutation carriers: a review;Bougie;Int. J. Surg. Oncol.,2011
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