(Q52185150)

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

1 reference

based on heuristic

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author name string

Maya-Núñez G

1

1 reference

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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