(Q59167809)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15349765%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

title

A novel mutation of WT1 exon 9 in a patient with Denys-Drash syndrome and pyloric stenosis (English)

1 reference

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1 January 2020

1 reference

1 reference

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2

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1 January 2020

author name string

Min Hu

1

1 reference

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1 January 2020

Neville Howard

3

1 reference

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1 January 2020

Alex Kan

4

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1 January 2020

Jeffrey Chaitow

5

1 reference

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1 January 2020

Dianne Little

6

1 reference

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1 January 2020

Stephen I Alexander

7

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1 January 2020

publication date

28 July 2004

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1 January 2020

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1 January 2020

volume

19

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1 January 2020

issue

10

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1 January 2020

page(s)

1160-1163

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https://scigraph.springernature.com/pub.10.1007/s00467-004-1564-3

1 January 2020

exact match

0 references

cites work

Mutation and cancer: statistical study of retinoblastoma

1 reference

12 December 2020

Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twins

1 reference

12 December 2020

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

1 reference

12 December 2020

A clinical overview of WT1 gene mutations

1 reference

12 December 2020

Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations

1 reference

12 December 2020

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

1 reference

12 December 2020

The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryo.

1 reference

12 December 2020

Congenital hypertrophic pyloric stenosis and associated anomalies in the genitourinary tract

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

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

1 reference

12 December 2020

Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome

1 reference

12 December 2020

Differential expression of the actin-binding proteins, alpha-actinin-2 and -3, in different species: implications for the evolution of functional redundancy.

1 reference

12 December 2020

Polymorphic and tissue-specific imprinting of the human Wilms tumor gene, WT1.

1 reference

12 December 2020

GONADOBLASTOMA ASSOCIATED WITH PURE GONADAL DYSGENESIS IN MONOZYGOUS TWINS.

1 reference

12 December 2020

Congenital mesoblastic nephroma, nephrocalcinosis, and hypertrophic pyloric stenosis

1 reference

12 December 2020

10.1007/S00467-004-1564-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15349765%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

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