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(1 - 4 of 4)
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration
Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers