(Q33890336)

29 July 2017

1 reference

title

Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy? (English)

1 reference

29 July 2017

1 reference

Koziell A

1

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29 July 2017

Charmandari E

2

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29 July 2017

Hindmarsh PC

3

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29 July 2017

Rees L

4

1 reference

29 July 2017

Scambler P

5

1 reference

29 July 2017

Brook CG

6

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29 July 2017

language of work or name

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1 April 2000

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29 July 2017

published in

Clinical Endocrinology

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29 July 2017

volume

52

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29 July 2017

issue

4

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29 July 2017

page(s)

519-524

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Donor splice-site mutations in WT1 are responsible for Frasier syndrome

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

Overlapping RNA and DNA binding domains of the wt1 tumor suppressor gene product

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

Software and database for the analysis of mutations in the human WT1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

21 January 2018

The Denys-Drash syndrome

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

Wilms' tumor 1 and Dax-1 modulate the orphan nuclear receptor SF-1 in sex-specific gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

Multiple drug resistance-related messenger RNA expression in archival formalin-fixed paraffin-embedded human breast tumour tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

Fine structure analysis of the WT1 gene in sporadic Wilms tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

Infrequent mutation of theWT1 gene in 77 Wilms' tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

Distinct molecular origins for Denys-Drash and Frasier syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00980.X

10.1046/J.1365-2265.2000.00980.X

21 January 2018

Identifiers

DOI

1 reference

29 July 2017

1 reference