Genomic organization of the human fibroblast growth factor receptor 2 (FGFR2) gene and comparative analysis of the human FGFR gene family (Q30669080)

26 June 2017

title

Genomic organization of the human fibroblast growth factor receptor 2 (FGFR2) gene and comparative analysis of the human FGFR gene family (English)

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26 June 2017

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Zhang Y

1

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26 June 2017

Gorry MC

series ordinal

2

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26 June 2017

Post JC

series ordinal

3

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26 June 2017

Ehrlich GD

series ordinal

4

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26 June 2017

language of work or name

English

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publication date

1 April 1999

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26 June 2017

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26 June 2017

volume

230

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26 June 2017

issue

1

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26 June 2017

page(s)

69-79

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Genomic structure of the downstream part of the human FLT3 gene: exon/intron structure conservation among genes encoding receptor tyrosine kinases (RTK) of subclass III

26 June 2017

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Multiple Interdependent Sequence Elements Control Splicing of a Fibroblast Growth Factor Receptor 2 Alternative Exon

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Fibroblast growth factor receptor 3 is a negative regulator of bone growth

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Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras

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Fibroblast growth factors, their receptors and receptor disorders

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Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson—Weiss syndrome

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Differential expression of the fibroblast growth factor receptor (FGFR) multigene family in normal human adult tissues

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Structural and Functional Diversity in the FGf Receptor Multigene Family

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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

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Genomic structure and complete sequence of the human FGFR4 gene

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Two gene duplication events in the human and primate dopamine D5 receptor gene family

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The heparan sulfate-fibroblast growth factor family: diversity of structure and function.

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Neuronal adhesion molecules signal through FGF receptor

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Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability

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Genomic organization of the human fibroblast growth factor receptor 3 (FGFR3) gene and comparative sequence analysis with the mouse Fgfr3 gene

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Unique expression pattern of the FGF receptor 3 gene during mouse organogenesis

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Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome

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7 January 2021

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

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Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes

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Identifiers

DOI

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26 June 2017

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