(Q48206248)

English

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour

scientific article published in October 1991

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

author name string

Pelletier J

1

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

Bruening W

2

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

Li FP

3

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

Haber DA

4

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

Glaser T

5

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

Housman DE

6

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

language of work or name

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publication date

1 October 1991

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

353

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

6343

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

431-434

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

ASSOCIATION OF WILMS'S TUMOR WITH ANIRIDIA, HEMIHYPERTROPHY AND OTHER CONGENITAL MALFORMATIONS

1 reference

https://api.crossref.org/works/10.1038%2F353431A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

1 reference

https://api.crossref.org/works/10.1038%2F353431A0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F353431A0

7 January 2021

based on heuristic

inferred from DOI database lookup

The candidate Wilms' tumour gene is involved in genitourinary development

1 reference

https://api.crossref.org/works/10.1038%2F353431A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of the Wilms' tumor gene WT1 in the murine urogenital system

1 reference

https://api.crossref.org/works/10.1038%2F353431A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2F353431A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.

1 reference

https://api.crossref.org/works/10.1038%2F353431A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13

1 reference

https://api.crossref.org/works/10.1038%2F353431A0

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

1 reference

https://api.crossref.org/works/10.1038%2F353431A0

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes

1 reference

https://api.crossref.org/works/10.1038%2F353431A0

7 January 2021

based on heuristic

inferred from DOI database lookup

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1038%2F353431A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/353431A0

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/1654525

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