1995•Nature GeneticsRequires access

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

Andrew O.M. Wilkie, Sarah F. Slaney, Michael Oldridge, Michael D. Poole, Geraldine J. Ashworth, Anthony D. Hockley, Richard Hayward, David J. David, Louise J. Pulleyn, Paul Rutland, S Malcolm, Robin M. Winter, William Reardon

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Key concepts: Apert syndrome, Craniosynostosis, Biology, Crouzon syndrome, Fibroblast growth factor receptor 2, Syndactyly, Missense mutation, Genetics

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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome — Research Paper | ScholarLens