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1. Cancer risks for other sites in addition to breast in CHEK2 c.1100delC families

3. Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study

7. Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study

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

9. 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).

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

14. STRAD in Peutz-Jeghers syndrome and sporadic cancers

15. Germline BRCA-Associated Endometrial Carcinoma Is a Distinct Clinicopathologic Entity

16. Lack of genotype-phenotype correlation in basal cell nevus syndrome: A Dutch multicenter retrospective cohort study

17. Alcohol Consumption, Cigarette Smoking, and Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Results from The BRCA1 and BRCA2 Cohort Consortium

18. Alcohol consumption, cigarette smoking, and risk of breast cancer for BRCA1 and BRCA2 mutation carriers: Results from the BRCA1 and BRCA2 cohort consortium.

19. Cancer risks for other sites in addition to breast in CHEK2c.1100delC families

20. Multiple fibroadenomas harbouring carcinoma in situ in a woman with a family history of breast/ovarian cancer. (Letters to JCP)

22. Novel strategies in newborn screening for cystic fibrosis: a prospective controlled study

23. Cost-effectiveness of newborn screening for cystic fibrosis determined with real-life data

25. TBX4 mutations (small patella syndrome) are associated with childhood-onset pulmonary arterial

26. Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney

27. Cystic fibrosis hielprik onderzoek bij pasgeborenen in Nederland : de Chopin studie eindrapport

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

30. Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study

31. Recurrence and variability of germline EPCAM deletions in Lynch syndrome

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

33. Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families

34. A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history.

35. A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example.

36. A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history

37. Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes.

44. A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

49. Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach.

50. Relative frequency and morphology of cancers in STK11 mutation carriers

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