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BRCA1/2 testing: uptake, phenocopies, and strategies to improve detection rates in initially negative families, , , , , , , , , and 7 other author(s). Clinical genetics, 82 (5): 478–483 (2012)Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA), , , , , , , , , and 123 other author(s). British journal of cancer, 101 (12): 2048–2054 (2009)The TP53 Arg72Pro and MDM2 309GT polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers, , , , , , , , , and 58 other author(s). British journal of cancer, 101 (8): 1456–1460 (2009)Strong evidence that the common variant S384F in BRCA2 has no pathogenic relevance in hereditary breast cancer, , , , , , , , and . Breast cancer research : BCR, 7 (5): R775-9 (2005)Association of hormone receptor status with grading, age of onset, and tumor size in BRCA1-associated breast cancer, , , , and . Virchows Archiv : an international journal of pathology, 454 (5): 519–524 (2009)An evaluation of the polymorphisms Ins16bp and Arg72Pro in p53 as breast cancer risk modifiers in BRCA1 and BRCA2 mutation carriers, , , , , , , , , and 21 other author(s). British journal of cancer, 99 (6): 974–977 (2008)