Von Hippel-Lindau disease

European Journal of Cancer

Volumn 30, Issue 13, 1994, Pages 1987-1990

  Maher, E R ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL FEATURE; GENE MUTATION; HUMAN; PRIORITY JOURNAL; REVIEW; VON HIPPEL LINDAU DISEASE;

CEREBELLAR NEOPLASMS; EYE NEOPLASMS; HEMANGIOBLASTOMA; HIPPEL-LINDAU DISEASE; HUMAN; MASS SCREENING; MUTATION; NEOPLASTIC SYNDROMES, HEREDITARY; RETINA;

EID: 0028077208     PISSN: 09598049     EISSN: None     Source Type: Journal    
DOI: 10.1016/0959-8049(94)00391-H     Document Type: Article

References (54)

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3. Familial renal cell carcinoma: clinical and molecular genetic aspects
4. Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma
5. Pheochromocytomas, Multiple Endocrine Neoplasia Type 2, and von Hippel-Lindau Disease
6. Clinical features and natural history of von Hippel-Lindau disease
7. Von Hippel-Lindau disease in a Newfoundland kindred
8. von Hippel-Lindau disease affecting 43 members of a single kindred
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10. Haemangioblastoma, haemangioblastomatosis, and von Hippel-Lindau disease
11. Renal lesions and pheochromocytoma in von Hippel-Lindau disease
12. von Hippel-Lindau disease and renal cell carcinoma in a 16-year-old boy
13. von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus
14. Islet cell tumors in von Hippel-Lindau disease: increased prevalence and relationship to the multiple endocrine neoplasias
15. von Hippel-Lindau disease: radiologic screening for visceral manifestations
16. Renal pathology in von Hippel-Lindau disease
17. The natural history of renal lesions in von Hippel-Lindau disease: a serial CT study in 28 patients
18. von Hippel-Lindau syndrome presenting as pancreatic endocrine insufficiency: a case report
19. Pancreatic cystadenoma in von Hippel-Lindau disease: an unusual cause of pancreatic and common bile duct obstruction
20. von Hippel-Lindau disease: clinical and pathological manifestations in nine families with 50 affected members
21. Germ cell tumor of testis in a patient with von Hippel-Lindau disease
22. Choroid plexus papilloma: a new presentation of von Hippel-Lindau diseae
23. Lindau's disease
24. Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of von Hippel Lindau disease
25. Evaluation of ulrasonographic diagnostic criteria for autosomal dominant polycystic disease 1
26. Ophthalmological screening for von Hippel-Lindau disease
27. Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markers
28. Screening for von Hippel-Lindau disease by DNA polymorphism analysis
29. Identification of the von Hippel-Lindau disease tumour suppressor gene
30. von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma
31. Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor gene
32. Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus
33. Mapping the von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis
34. Von Hippel-Lindau disease: identification of deletion mutations by pulsed-field gel electrophoresis
35. Localization of the von Hippel-Lindau disease gene to a small region of chromosome 3
36. Localization of the gene for von Hippel-Lindau disease to a small region of chromosome 3p by genetic linkage analysis
37. Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromsome 3p25-26
38. Three polymorphic dinucleotide repeats near the von Hippel Lindau (VHL) disease gene on human chromosome 3: D3S587; D3S1317; D3S1435
39. Dinucleotide repeat polymorphisms in the VHL region of human chromsome 3p25
40. TaqI and PstI RFLPs in the von Hippel-Lindau disease gene
41. A PCR generated AccI RFLP in the 3′ untranslated region of the von Hippel — Lindau disease (VHL) tumour suppressor gene
42. Detailed mapping of germline deletions of the von Hippel-Lindau disease tumour suppressor gene
43. Identification of intragenic mutations in the von Hippel-Landau disease tumour suppressor gene and correlation with disease phenotype
44. Molecular genetic investigations of the mechanism of tumourigenesis in von Hippel-Lindau disease: analysis of allele loss in VHL tumours
45. Specific genetic change in tumors associated with von Hippel-Lindau disease
46. A detailed deletion mapping of the short arm of chromosome 3 in sporadic renal cell carcinoma
47. The region of common allelic losses in sporadic renal cell carcinoma is bordered by the loci D3S2 and THRB
48. Molecular genetic investigation of sporadic renal cell carcinoma: analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22
49. Mutations of the VHL tumour suppressor gene in renal carcinoma
50. Positional cloning of the hereditary renal carcinoma 3;8 chromosome translocation breakpoint
51. A tumour suppressor locus within 3p14-p12 mediates rapid cell death of renal cell carcinoma in vivo
52. Antioncogenes and human cancer
53. Report of the committee on chromosome and gene loss in human neoplasia