(Q30338283)

Laura Arbour

2

0 references

Michael Stratton

8

Michael R. Stratton

0 references

Steven A. Narod

9

Steven A. Narod

0 references

Kathryn Pritchard-Jones

7

Kathryn Pritchard-Jones

0 references

author name string

Patricia Tonin

3

0 references

Jane Renshaw

4

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Jerry Pelletier

5

0 references

Sylvain Baruchel

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

6

0 references

language of work or name

English

0 references

publication date

August 1996

0 references

published in

Nature Genetics

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volume

13

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issue

4

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page(s)

461-463

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

Wilms' tumor in the Li-Fraumeni cancer family syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

The Bloom's syndrome gene product is homologous to RecQ helicases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

The human insulin-like growth factor-binding protein 4 gene maps to chromosome region 17q12-q21.1 and is close to the gene for hereditary breast-ovarian cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

Familial predisposition to Wilms tumor does not segregate with the WT1 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

7 January 2021

Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

7 January 2021

The relationship between nephroblastoma and neurofibromatosis (Von Recklinghausen's disease)

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

7 January 2021

Genetics of breast and ovarian cancer

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

7 January 2021

Wilms tumor in three patients with Bloom syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

7 January 2021

The Perlman syndrome: Familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

7 January 2021

Testing genomic imprinting in Wilm's tumor.

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

7 January 2021

Computer-simulation methods in human linkage analysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0896-461

7 January 2021