33 results on '"Menko, F H"'
Search Results
2. Screening for Hereditary Non-polyposis Colorectal Cancer in the Netherlands
3. Risk of spontaneous pneumothorax due to air travel and diving in patients with Birt–Hogg–Dubé syndrome
4. Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers
5. Bilateral Renal Tumour as Indicator for Birt-Hogg-Dubé Syndrome
6. Highly variable clinical manifestations in a large family with a novel GATA2 mutation
7. Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families
8. Absence of the Birt–Hogg–Dubé gene product is associated with increased hypoxia-inducible factor transcriptional activity and a loss of metabolic flexibility
9. Informing family members about a hereditary predisposition to cancer: attitudes and practices among clinical geneticists
10. TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes
11. Investigation of the Birt-Hogg-Dube tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer
12. Molecular profile of ductal carcinoma in situ of the breast in BRCA1 and BRCA2 germline mutation carriers
13. A case of loss of heterozygosity in the BRCA2 gene of a borderline ovarian tumor: case report and review of literature
14. Is surveillance of the small bowel indicated for Lynch syndrome families?
15. Re: Germline BRCA1 Mutations and a Basal Epithelial Phenotype in Breast Cancer
16. Expression of differentiation and proliferation related proteins in epithelium of prophylactically removed ovaries from women with a hereditary female adnexal cancer predisposition
17. PROPHYLACTIC SURGERY IN WOMEN AT HIGH RISK FOR BREAST AND/OR OVARIAN/TUBAL CANCER
18. HUMORAL IMMUNE RESPONSES TO MUC1 IN WOMEN WITH BRCA1/BRCA2 MUTATIONS
19. Histopathologic Features of Genetically Determined Ovarian Cancer
20. Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach
21. Atypical MEN Type 2B Associated with Two Germline RET Mutations on the Same Allele Not Involving Codon 918
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
24. Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2
25. The risk of brain tumours in hereditary non-polyposis colorectal cancer (HNPCC)
26. Clinical heterogeneity of familial colorectal cancer and its influence on screening protocols.
27. Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcifications
28. Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcifications
29. Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype.
30. Reply to Dr. Qumsiyeh
31. A giant congenital orbital tumor: An unusual presentation of retinoblastoma
32. Robin sequence and a deficiency of the left forearm in a girl with a deletion of chromosome 4q33-qter
33. Williams syndrome and chromosome 18.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.