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175 results on '"Bourdon V"'

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

3. Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature Communications, (2021), 12, 1, (1078), 10.1038/s41467-020-20496-3).

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

5. Rare germline large rearrangements in the BRCA1/2 genes and eight candidate genes in 472 patients with breast cancer predisposition

8. 645P Prediction of BRCA2 mutations in prostate cancer patients according early onset, metastatic phenotypes or family history of breast/ovary cancer

11. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

12. The contribution of germline rearrangements to the spectrum of BRCA2 mutations

13. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.

14. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

16. Novel diagnostic guidelines for prediction of variant spliceogenicity derived from a set of 311 combined in silico and in vitro studies: an international collaborative effort

17. Discrete, water-soluble, hetero-metallic chalcogenide oligomers as building blocks for functional films

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

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

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

22. Familial hematological malignancies: ASXL1 gene investigation

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

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

26. Progres recents dans les analyses genetiques d’identification

27. Risk based evaluation of the weight of DNA evidence

28. Molecular study of the perforin gene in familial hematological malignancies

29. Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

30. Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.

31. Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP

37. Rare germline large rearrangements in the BRCA1/ 2 genes and eight candidate genes in 472 patients with breast cancer predisposition.

42. Sur La Clearance Urinaire De La Noradrénaline Chez L'Homme

43. The release of glandular kallikrein from submaxillary glands of rats exposed to heat

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