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202 results on '"Gauthier-Villars M"'

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1. Retinoblastoma

6. Retinoblastoma

11. Malformations, Genetic Abnormalities, and Wilms Tumor

12. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

13. Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers

14. Le rétinoblastome

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

20. Comment les parents perçoivent-ils la prise en charge de leur enfant atteint de rétinoblastome ?

21. Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

22. Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

23. A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers

24. Diagnosis of Constitutional Mismatch Repair-deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents

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

26. Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers

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

28. Breast and ovarian cancer predisposition due to de novo BRCA1 and BRCA2 mutations

29. Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS families

32. Malformations, genetic abnormalities, and wilms tumor

33. Short-term psychological impact of the BRCA1/2 test result in women with breast cancer according to their perceived probability of genetic predisposition to cancer

36. Mosaicism for oncogenic G12D KRAS mutation associated with epidermal nevus, polycystic kidneys and rhabdomyosarcoma

38. Estimation du risque de cancer du sein dans une cohorte prospective de femmes porteuses d’une mutation sur les gènes BRCA : cohorte nationale GENEPSO

39. Common genetic variants and modification of penetrance of BRCA2-associated breast cancer

40. Retinoblastoma

42. Comprehensive screening for constitutional RB1 mutations by DHPLC and QMPSF

43. Diagnostic des patientes à risque de cancer du sein.

44. Breast and ovarian cancer predisposition due to de novo BRCA1and BRCA2mutations

45. Beckwith-Wiedemann Syndrome: Growth Pattern and Tumor Risk according to Molecular Mechanism, and Guidelines for Tumor Surveillance.

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

47. Mutation screening of the RB1 gene in 192 retinoblastoma patients.

48. Cholestasis in children with portal vein obstruction

49. Patients' characteristics and rate of Internet use to obtain cancer information.

50. Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

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