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Your search keyword '"Tapper, William J"' showing total 28 results

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Start Over You searched for: Author "Tapper, William J" Remove constraint Author: "Tapper, William J" Publisher univ cambridge, ctr canc genet epidemiol, dept oncol, cambridge, england. Remove constraint Publisher: univ cambridge, ctr canc genet epidemiol, dept oncol, cambridge, england.
28 results on '"Tapper, William J"'

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1. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

2. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

3. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

4. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

5. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

6. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

7. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

8. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

9. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

10. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

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

12. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

13. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

14. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

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

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

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

18. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

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

20. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

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

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

23. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

24. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

25. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

26. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

27. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

28. Genome-wide association study of germline variants and breast cancer-specific mortality

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