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3. Functional structural and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients

4. The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma

9. Contribution of CDKN2A/P16, P14, CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanoma.

10. Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16INK4A, P14ARF or cdk4 genes.

13. Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

14. High frequency of germline SUFU mutations in children with desmoplastic/nodular medulloblastoma younger than 3 years of age.

15. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma.

16. Four novel RET germline variants in exons 8 and 11 display an oncogenic potential in vitro.

17. Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients.

18. The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma.

19. Hereditary breast cancer associated with a germline BRCA2 mutation in identical female twins with similar disease expression.

20. Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group.

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