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4. Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling

5. Patients’ experiences with pre-test genetic counseling provided by breast cancer healthcare professionals: Results from a large prospective multicenter study

8. Barriers to genetic testing in clinical psychiatry and ways to overcome them: from clinicians' attitudes to sociocultural differences between patients across the globe

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

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

18. Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)

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

25. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

26. Oral Contraceptive Use and Breast Cancer Risk: Retrospective and Prospective Analyses From a BRCA1 and BRCA2 Mutation Carrier Cohort Study

27. The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations

28. Expertise van klinisch geneticus beter benutten

29. DNA-diagnostiek bij dementie

32. Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers

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

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

35. Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

36. A multicentre comparative prospective blinded analysis of EUS and MRI for screening of pancreatic cancer in high-risk individuals

37. Lust en last binnen de klinische genetica

38. DNA-diagnostiek bij erfelijke kanker: het belang van betrouwbare familiegegevens

39. Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

40. Reproductieve erfelijkheidsadvisering tijdens de zwangerschap: het belang van (vroeg)tijdige verwijzing

41. Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers : results from a multicenter study

42. Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2

43. Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers : Implications for risk prediction

44. Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

46. A multicentre comparative prospective blinded analysis of EUS and MRI for screening of pancreatic cancer in high-risk individuals.

47. Erfelijkheidsadvisering: mag bijzaak hoofdzaak worden?

48. Parental somatic and germ-line mosaicism for a FBN2 mutation and analysis of FBN2 transcript levels in dermal fibroblasts

49. Erfelijkheidsadvisering: mag bijzaak hoofdzaak worden?

50. Het Smith-Lemli-Opitz-syndroom; een bijzonder defect in het cholesterolmetabolisme

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