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3. Germline variant affecting p53β isoforms predisposes to familial cancer

5. Real-world routine diagnostic molecular analysis for TP53 mutational status is recommended over p53 immunohistochemistry in B-cell lymphomas

6. Molecular and Clinicopathologic Characterization of Mismatch Repair-Deficient Endometrial Carcinoma Not Related to MLH1 Promoter Hypermethylation

7. Impact of genetic counseling strategy on diagnostic yield and workload for genome-sequencing-based tumor diagnostics

8. MLH1 Promotor Hypermethylation in Colorectal and Endometrial Carcinomas from Patients with Lynch Syndrome

9. Loss of bone morphogenetic protein signaling in fibroblasts results in CXCL12-driven serrated polyp development

11. Molecular Profile of MSH6-Associated Colorectal Carcinomas Shows Distinct Features From Other Lynch Syndrome–Associated Colorectal Carcinomas

13. Clinicogenomic associations in childhood Langerhans cell histiocytosis: an international cohort study

21. Molecular analysis using SalvGlandDx improves risk of malignancy estimation and diagnosis of salivary gland cytopathology: An exploratory multicenter study

22. Frequent mutated B2M, EZH2, IRF8, and TNFRSF14 in primary bone diffuse large B-cell lymphoma reflect a GCB phenotype

25. RET Fluorescence In Situ Hybridization Analysis Is a Sensitive but Highly Unspecific Screening Method for RET Fusions in Lung Cancer

28. Optimizing Mutation and Fusion Detection in NSCLC by Sequential DNA and RNA Sequencing

29. Comprehensive diagnostics of acute myeloid leukemia by whole transcriptome RNA sequencing

30. MLH1 Promotor Hypermethylation in Colorectal and Endometrial Carcinomas from Patients with Lynch Syndrome

31. BRAF V600E is associated with higher incidence of second cancers in adults with Langerhans cell histiocytosis

32. Impact of genetic counselling strategy on diagnostic yield and workload for genome sequencing-based tumour diagnostics

33. Robust detection of translocations in lymphoma FFPE samples using targeted locus capture-based sequencing

38. Recommendations for the clinical interpretation and reporting of copy number gains using gene panel NGS analysis in routine diagnostics

39. Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13

43. Molecular Profile of MSH6-Associated Colorectal Carcinomas Shows Distinct Features From Other Lynch Syndrome–Associated Colorectal Carcinomas

44. QPOLE: A Quick, Simple, and Cheap Alternative for POLE Sequencing in Endometrial Cancer by Multiplex Genotyping Quantitative Polymerase Chain Reaction

45. MLH1Promotor Hypermethylation in Colorectal and Endometrial Carcinomas from Patients with Lynch Syndrome

47. Somatic POLE proofreading domain mutation, immune response, and prognosis in colorectal cancer: a retrospective, pooled biomarker study

48. SNP association study in PMS2-associated Lynch syndrome

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