(Q47775632)

5 February 2018

review article

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title

Molecular genetic analysis of von Hippel-Lindau disease (English)

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5 February 2018

author name string

Richards FM

1

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5 February 2018

Webster AR

2

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5 February 2018

McMahon R

3

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5 February 2018

Woodward ER

4

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5 February 2018

Rose S

5

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5 February 2018

Maher ER

6

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5 February 2018

language of work or name

English

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publication date

1 June 1998

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5 February 2018

Journal of Internal Medicine

published in

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5 February 2018

volume

243

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5 February 2018

issue

6

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5 February 2018

page(s)

527-533

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5 February 2018

The von Hippel-Lindau tumor suppressor gene. A rare and intriguing disease opening new insight into basic mechanisms of carcinogenesis

cites work

1 reference

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Von Hippel-Lindau disease: a genetic study

21 January 2018

1 reference

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Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease gene.

21 January 2018

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Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Clustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locus

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Clinical features and molecular genetics of Von Hippel-Lindau disease

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Identification of the von Hippel-Lindau disease tumor suppressor gene

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Uptake of genetic testing for cancer predisposition.

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Localization of the von Hippel-Lindau disease gene to a small region of chromosome 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

A PCR generated AccI RFLP in the 3' untranslated region of the von Hippel-Lindau disease (VHL) tumour suppressor gene

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlations with phenotype

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Presymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markers

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

A genetic register for von Hippel-Lindau disease

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Detailed mapping of germline deletions of the von Hippel-Lindau disease tumour suppressor gene

21 January 2018

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Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype

21 January 2018

1 reference

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Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effect

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Genotype-phenotype correlation in von Hippel-Lindau disease: identification of a mutation associated with VHL type 2A

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2796.1998.00334.X

10.1046/J.1365-2796.1998.00334.X

21 January 2018

Identifiers

DOI

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5 February 2018

1 reference

5 February 2018