(Q24314986)

skeletal system development

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

M Muenke

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U Schell

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A Hehr

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N H Robin

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H W Losken

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A Schinzel

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L J Pulleyn

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P Rutland

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W Reardon

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S Malcolm

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

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language of work or name

English

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publication date

November 1994

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269-74

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG1194-269

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG1194-269

A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10.

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

Two craniosynostotic syndrome loci, Crouzon and Jackson-Weiss, map to chromosome 10q23-q26

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

Diverse forms of a receptor for acidic and basic fibroblast growth factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

Signal transduction by allosteric receptor oligomerization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

The structure and expression of the FGF receptor-1 mRNA isoforms in rat tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

The human fibroblast growth factor receptor genes: a common structural arrangement underlies the mechanisms for generating receptor forms that differ in their third immunoglobulin domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

Dominant erbliche Akrocephalosyndaktylie

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021

Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021

Pitfalls of genetic counselling in Pfeiffer's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021

Complete sequence of a human receptor for acidic and basic fibroblast growth factors

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021

Isolation of an additional member of the fibroblast growth factor receptor family, FGFR-3

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021

A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4.

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021

Signal transduction by receptors with tyrosine kinase activity

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021

Identification of a developmentally regulated protein-tyrosine kinase by using anti-phosphotyrosine antibodies to screen a cDNA expression library

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021

A murine fibroblast growth factor (FGF) receptor expressed in CHO cells is activated by basic FGF and Kaposi FGF

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021

Improvement of PCR amplified DNA sequencing with the aid of detergents

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-269

7 January 2021