(Q33767043)

29 July 2017

1 reference

title

SHOX: pseudoautosomal homeobox containing gene for short stature and dyschondrosteosis (English)

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29 July 2017

Ogata T

1

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29 July 2017

language of work or name

1 reference

1 June 1999

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Growth Hormone & I G F Research

29 July 2017

published in

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29 July 2017

volume

9 Suppl B

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29 July 2017

page(s)

53-7; discussion 57-8

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The pseudoautosomal regions of the human sex chromosomes

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2899%2980082-3

7 January 2021

Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2899%2980082-3

7 January 2021

Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2899%2980082-3

7 January 2021

Short stature in a girl with partial monosomy of the pseudoautosomal region distal to DXYS15: further evidence for the assignment of the critical region for a pseudoautosomal growth gene(s).

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2899%2980082-3

7 January 2021

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2899%2980082-3

7 January 2021

Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2899%2980082-3

7 January 2021

SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2899%2980082-3

7 January 2021

Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2899%2980082-3

7 January 2021

An interspersed repeated sequence specific for human subtelomeric regions

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2899%2980082-3

7 January 2021

Madelung's deformity. A follow-up study of 26 cases and a review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2899%2980082-3

7 January 2021

10.1016/S1096-6374(99)80082-3

Identifiers

DOI

1 reference

29 July 2017

1 reference