Leiden University Scholarly Publications

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Rare Mutations in RINT1 Predispose Carriers to Breast and Lynch Syndrome-Spectrum Cancers
Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles
Rare Mutations in XRCC2 Increase the Risk of Breast Cancer
Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the breast cancer association consortium studies