Associated Papers
Genotypic and phenotypic analysis of familial male breast cancer shows under representation of the HER2 and basal subtypes in BRCA-associated carcinomas.
Deb S et al.
Bmc Cancer, 2012
Familial concordance of breast cancer pathology as an indicator of genotype in multiple-case families.
Balleine RL et al.
Genes, Chromosomes & Cancer, 2010
Histopathological features of 'BRCAX' familial breast cancers in the kConFab resource.
Loughrey M et al.
Pathology, 2008
BRCA1 and BRCA2 missense variants of high and low clinical significance influence lymphoblastoid cell line post-irradiation gene expression.
Waddell N et al.
Plos Genetics, 2008
18497862 (PubMed )
Supplement: pgen.1000080.s002.xls › Sheet1
Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics.
Scott CL et al.
Human Genetics, 2003
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