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Your search keyword '"Gillanders, E.M."' showing total 15 results

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2. Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

3. The value of molecular haplotypes in a family-based linkage study

4. Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (vol 9, 4774, 2018)

5. Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

8. Genome-wide association study identifies three new melanoma susceptibility loci

9. Genome-wide association study identifies three loci associated with melanoma risk

10. A variant in FTO shows association with melanoma risk not due to BMI

11. A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment

13. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome

14. Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33

15. Gene-environment interactions in cancer epidemiology: A national cancer institute think tank report

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