Acronym	Definition
FGFR2	Fibroblast Growth Factor Receptor 2 (also seen as FGFR-2)

References in periodicals archive

et al., "Fibroblast growth factor receptor 2 tyrosine kinase fusions define a unique molecular subtype of cholangiocarcinoma", Hepatology, 2014, 59, 1427-1434.

Eisai: Japan MHLW Grants Sakigake Designation to Novel Fibroblast Growth Factor (FGF) Receptor Selective Tyrosine Kinase Inhibitor E7090

To the Editor: Crouzon Syndrome (CS), also known as craniosynostosis, is an autosomal dominant genetic disorder linked to single-gene mutation of fibroblast growth factor receptor 2 ( FGFR2 ).[1],[2],[3] The premature fusion of certain skull bones results in a serial of dysmorphic features including underdeveloped maxilla, protruded mandible, shallow orbits, proptosis, and beaked nose.

Crouzon Syndrome Associated with Congenital Coarctation of Aorta

Breathnach, "Control of BEK and K-SAM splice sites in alternative splicing of the fibroblast growth factor receptor 2 pre-mRNA," Molecular and Cellular Biology, vol.

The Role of Fibroblast Growth Factors in Tooth Development and Incisor Renewal

Mutations in the FGFR2 gene located on 10q26 that encode fibroblast growth factor receptor 2 is responsible for a part of the syndromic craniosynostosis.

FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis

Fibroblast Growth Factor Receptor 2 [OMIM database on the Internet].

Analisis molecular de los exones 8, 9 y 10 del gen del factor de crecimiento de fibroblastos (FGFR2) en dos familias con casos indice de sindrome de Apert.

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