Re: differential effects of FGFR2 mutation in ophthalmologic findings in Apert syndrome

J Craniofac Surg. 2007 Mar;18(2):459-60. doi: 10.1097/01.scs.0000249354.81967.d9.

Authors

Matthew D Kwan¹, Derrick C Wan, H Peter Lorenz, Michael T Longaker

Affiliation

¹ Children's Surgical Research Program, Division of Plastic and Reconstructive Surgery, Department of Surgery, Stanford University School of Medicine, Stanford, California 94305-5148, USA.

PMID: 17414305
DOI: 10.1097/01.scs.0000249354.81967.d9

No abstract available

Publication types

Comment

MeSH terms

Acrocephalosyndactylia / complications
Acrocephalosyndactylia / genetics*
Amino Acid Substitution
DNA Mutational Analysis
Eye Abnormalities / etiology
Eye Abnormalities / genetics*
Humans
Mutation, Missense
Receptor, Fibroblast Growth Factor, Type 2 / genetics*

Substances

Receptor, Fibroblast Growth Factor, Type 2