23 results on '"Menko, F H"'
Search Results
2. Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D)
3. Highly variable clinical manifestations in a large family with a novel GATA2 mutation
4. Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations
5. Absence of the Birt-Hogg-Dubeé gene product is associated with increased hypoxia-inducible factor transcriptional activity and a loss of metabolic flexibility
6. Perceiving cancer-risks and heredity-likelihood in genetic-counseling: how counselees recall and interpret BRCA 1/2-test results
7. Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis
8. Molecular profile of ductal carcinoma in situ of the breast in BRCA1 and BRCA2 germline mutation carriers
9. Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes
10. Genetic defects underlying Peutz–Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates
11. Is surveillance of the small bowel indicated for Lynch syndrome families?
12. STK11 status and intussusception risk in Peutz-Jeghers syndrome
13. Distinction between hereditary and sporadic breast cancer on the basis of clinicopathological data
14. STRAD in Peutz-Jeghers syndrome and sporadic cancers
15. Cancer risks in BRCA2 families: estimates for sites other than breast and ovary
16. Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)
17. Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2
18. Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect
19. Expression of differentiation and proliferation related proteins in epithelium of prophylactically removed ovaries from women with a hereditary female adnexal cancer predisposition
20. Rapidly progressive adenomatous polyposis in a patient with germline mutations in both the APC and MLH1 genes: the worst of two worlds
21. Experience of discharge from colonoscopy of mutation negative HNPCC family members
22. MSH2 Mutation Carriers Are at Higher Risk of Cancer Than MLH1 Mutation Carriers: A Study of Hereditary Nonpolyposis Colorectal Cancer Families
23. Accumulation of p53 protein is frequent in ovarian cancers associated with BRCA1 and BRCA2 germline mutations
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