Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene. (Q52185150)

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scientific article published in June 1998

Language	Label	Description	Also known as
English	Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene.	scientific article published in June 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene. (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

Contiguous gene syndrome

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based on heuristic

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author name string

Maya-Núñez G

1

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Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

Cuevas-Covarrubias S

2

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

Zenteno JC

3

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

Ulloa-Aguirre A

4

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

Kofman-Alfaro S

5

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

Méndez JP

6

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

publication date

1 June 1998

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Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

number of pages

6

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Clinical Endocrinology

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Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

48

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Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

6

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

713-718

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

Screening for steroid sulfatase (STS) gene deletions by multiplex DNA amplification

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

A clinical and genetic study of X-linked recessive ichthyosis and contiguous gene defects

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL gene.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

Long-range restriction map of the terminal part of the short arm of the human X chromosome

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

The Kallmann syndrome gene product expressed in COS cells is cleaved on the cell surface to yield a diffusible component

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

Deletion analysis maps ocular albinism proximal to the steroid sulphatase locus

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.1998.00406.X

21 January 2018

Identifiers

10.1046/J.1365-2265.1998.00406.X

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 April 2018

http://europepmc.org/abstract/MED/9713559

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