๐”– Bobbio Scriptorium
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Fibroblast Growth Factor Receptor-2 Mutations in Craniosynostosis

โœ Scribed by Sue Malcolm; William Reardon


Book ID
119873779
Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
437 KB
Volume
785
Category
Article
ISSN
0890-6564

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Fibroblast growth factor receptor (FGFR) mutations have been found in craniosynostosis syndromes with and without limb and/ or dermatologic anomalies. Ocular manifestations of FGFR2 syndromes are reported to include shallow orbits, proptosis, strabismus, and hypertelorism, but no ocular anterior cha