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Your search keyword '"Rebbeck, Tim"' showing total 3 results

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1. Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.

2. Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.

3. Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers.

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