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Fibroblast growth factor receptor mutations and craniosynostosis: Three receptors, five syndromes

โœ Scribed by Andrew O. M. Wilkie


Book ID
112882114
Publisher
Springer-Verlag
Year
1996
Tongue
English
Weight
335 KB
Volume
63
Category
Article
ISSN
0019-5456

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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