(Q28240083)

1

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E Zanaria

2

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S Guioli

3

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G Floridia

4

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K C Worley

5

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G Tonini

6

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E Ferrante

7

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G Chiumello

8

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E R McCabe

9

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M Fraccaro

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

10

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language of work or name

English

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publication date

August 1994

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published in

Nature Genetics

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volume

7

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issue

4

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page(s)

497-501

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0894-497

Report of a kindred with X-linked (or autosomal dominant sex-limited) 46,XY partial gonadal dysgenesis

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

Yeast artificial chromosome cloning in the glycerol kinase and adrenal hypoplasia congenita region of Xp21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

Genetic evidence equating SRY and the testis-determining factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

A high resolution deletion map of human chromosome Xp22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

Genetically Determined Sex-Reversal in 46,XY Humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

7 January 2021

Sex reversal in a child with a 46,X,Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

7 January 2021

Probable inverted tandem duplication of Xp in a 46,Xp+Y boy

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

7 January 2021

Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

7 January 2021

Identification of new markers in Xp21 between DXS28 (C7) and DMD

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

7 January 2021

A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

7 January 2021

Clinical and Pathologic Spectrum of 46,XY Gonadal Dysgenesis

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

7 January 2021

DNA Binding Activity of Recombinant SRY from Normal Males and XY Females

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

7 January 2021

Dominant negative mutations in the Wilms tumour (WT1) gene cause Denys-Drash syndrome--proof that a tumour-suppressor gene plays a crucial role in normal genitourinary development

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

7 January 2021

High resolution R- and G-banding on the same preparation

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

7 January 2021

A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphisms.

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-497

7 January 2021

Identifiers

DOI

10.1038/NG0894-497

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

7951319

1 reference

Consolidated OpenCitations Corpus – April 2017