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1. Supplementary Tables 1-4 from Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

2. Data from Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

3. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

4. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

5. Common breast cancer risk loci predispose to distinct tumor subtypes

6. Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

7. Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

8. Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

10. DNA adducts, DNA repair genotype/phenotype and cancer risk

11. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.

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