(Q58062406)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262521%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

von Hippel-Lindau disease: identification of deletion mutations by pulsed-field gel electrophoresis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262521%20AND%20SRC:MED&resulttype=core&format=json

von Hippel-Lindau disease

28 October 2019

main subject

1 reference

M Yao

1

1 reference

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28 October 2019

F Latif

2

1 reference

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28 October 2019

M L Orcutt

3

1 reference

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28 October 2019

I Kuzmin

4

1 reference

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28 October 2019

T Stackhouse

5

1 reference

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28 October 2019

F W Zhou

6

1 reference

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28 October 2019

K Tory

7

1 reference

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28 October 2019

F M Duh

8

1 reference

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28 October 2019

F Richards

9

1 reference

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28 October 2019

E Maher

10

1 reference

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28 October 2019

language of work or name

English

0 references

publication date

1 December 1993

1 reference

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28 October 2019

1 reference

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28 October 2019

volume

92

1 reference

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28 October 2019

page(s)

605-614

1 reference

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28 October 2019

issue

6

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00420947

28 October 2019

exact match

0 references

cites work

Mapping of Von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis

1 reference

12 December 2020

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

Von Hippel-Lindau disease: a genetic study

1 reference

12 December 2020

Specific genetic change in tumors associated with von Hippel-Lindau disease

1 reference

12 December 2020

Confirmation of linkage in von Hippel-Lindau disease

1 reference

12 December 2020

von Hippel-Lindau syndrome: cloning and identification of the plasma membrane Ca(++)-transporting ATPase isoform 2 gene that resides in the von Hippel-Lindau gene region

1 reference

12 December 2020

Polymerase chain reaction (PCR) for detection of HindIII polymorphism at the D3F15S2 locus

1 reference

12 December 2020

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

1 reference

12 December 2020

Current methods for YAC clone characterization

1 reference

12 December 2020

A new polymorphic probe on chromosome 3p: lambda LIB19-63' (D3S601).

1 reference

12 December 2020

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

1 reference

12 December 2020

Construction of long-range restriction maps in human DNA using pulsed field gel electrophoresis

1 reference

12 December 2020

Identification of deletion mutations and three new genes at the familial polyposis locus

1 reference

12 December 2020

Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents

1 reference

12 December 2020

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

1 reference

12 December 2020

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

1 reference

12 December 2020

Genetics of human cancer

1 reference

12 December 2020

Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis

1 reference

12 December 2020

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

1 reference

12 December 2020

Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma

1 reference

12 December 2020

von Hippel-Lindau disease affecting 43 members of a single kindred

1 reference

12 December 2020

Structural gene coding for multifunctional protein carrying orotate phosphoribosyltransferase and OMP decarboxylase activity is located on long arm of human chromosome 3.

1 reference

12 December 2020

cA479 (D3S719): a cosmid mapped telomeric of the Von Hippel Lindau disease gene contains the D3S18 locus

1 reference

12 December 2020

LINDAU'S DISEASE. REVIEW OF THE LITERATURE AND STUDY OF A LARGE KINDRED.

1 reference

12 December 2020

A genetic linkage map of 96 loci on the short arm of human chromosome 3.

1 reference

12 December 2020

Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma

1 reference

12 December 2020

Segregation and linkage analyses of von Hippel Lindau disease among 220 descendants from one kindred

1 reference

12 December 2020

Screening for von Hippel-Lindau disease by DNA polymorphism analysis

1 reference

12 December 2020

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

1 reference

12 December 2020

High-resolution chromosome banding and fragile site studies in von Hippel-Lindau syndrome

1 reference

12 December 2020

Light and electron microscopic study of early lesions in angiomatosis retinae

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00420947

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8262521%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference