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1. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

2. Reply to Kratz et al.

3. Guidelines for the Li–Fraumeni and heritable TP53-related cancer syndromes

4. Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

5. The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations

6. The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations

7. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

8. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

9. Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

10. Tumours with loss of MSH6 expression are MSI-H when screened with a pentaplex of five mononucleotide repeats

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