(Q34283729)

1 August 2017

title

Exclusion of WTAP and HOXA13 as candidate genes for isolated hypospadias (English)

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1 August 2017

Boris Utsch

1

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author name string

Ali Kaya

2

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1 August 2017

Atila Ozburun

3

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1 August 2017

Michael J Lentze

4

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1 August 2017

Norbert Albers

5

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1 August 2017

Michael Ludwig

6

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1 August 2017

publication date

1 January 2003

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Scandinavian Journal of Urology and Nephrology

1 August 2017

published in

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1 August 2017

volume

37

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1 August 2017

issue

6

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1 August 2017

page(s)

498-501

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The molecular basis of male sexual differentiation

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

Sexual differentiation and environmental endocrine disrupters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

Mutations inSRY andSOX9: Testis-determining genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

Naturally occurring mutations of the luteinizing hormone receptor gene affecting reproduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

The molecular basis of androgen insensitivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length?

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

Infertility in adult hypodactyly mice is associated with hypoplasia of distal reproductive structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

WT-1 is required for early kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

A clinical overview of WT1 gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00365590310014517

10.1080/00365590310014517

21 January 2018

Identifiers

DOI

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1 August 2017

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