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2. Dominantly inherited micro-satellite instable cancer – the four Lynch syndromes - an EHTG, PLSD position statement

3. Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statement

4. Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database

8. Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

9. Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study

10. Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

11. Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

14. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

16. Characterization of rare germline variants in familial multiple myeloma

17. A functional assay–based procedure to classify mismatch repair gene variants in Lynch syndrome

20. AXIN2‐related oligodontia‐colorectal cancer syndrome with cleft palate as a possible new feature

21. PMS2-associated Lynch syndrome: Past, present and future

22. Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

25. Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma

26. Is HLA type a possible cancer risk modifier in Lynch syndrome?

27. Is HLA type a possible cancer risk modifier in Lynch syndrome?

29. Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

30. Is HLA type a possible cancer risk modifier in Lynch syndrome?

31. Additional file 1 of Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

32. Incidence of and survival after subsequent cancers in carriers of pathogenic MMR variants with previous cancer: a report from the prospective Lynch syndrome database

33. Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database

35. Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma.

37. Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown Significance

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

40. Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum

41. Encyclopaedia of tumour-associated familial disorders. Part I: from AIMAH to CHIME syndrome

42. Clinical and genetic aspects of testicular germ cell tumours

43. Familial Multiple Myeloma: Report on Two Families and Discussion of Screening Options

46. Variation in the Risk of Colorectal Cancer for Lynch Syndrome: A retrospective family cohort study

47. Familial Cervical Cancer: Case Reports, Review and Clinical Implications

48. Erratum: Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

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