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Breast cancer genetics. Implications of clinical practice.
BRCA2 T2722R is a deleterious allele that causes exon skipping.
Breast cancer genetics in African Americans.
Genetic testing in an ethnically diverse cohort of high-risk women: a comparative analysis of BRCA1 and BRCA2 mutations in American families of European and African ancestry.
BRCA1 promoter methylation in sporadic breast cancer is associated with reduced BRCA1 copy number and chromosome 17 aneusomy.
Complete allelic analysis of BRCA1 and BRCA2 variants in young Nigerian breast cancer patients.
Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations.
Aberrant RNA splicing and its functional consequences in cancer cells.
Evidence for an ancient BRCA1 mutation in breast cancer patients of Yoruban ancestry.
Searching for large genomic rearrangements of the BRCA1 gene in a Nigerian population.
Genetic anticipation in BRCA1/BRCA2 families after controlling for ascertainment bias and cohort effect.