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Nature Genetics 9, 165–172 (1 February 1995) | doi:10.1038/ng0295-165

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 D. Hayward , David J. David , Louise J. Pulleyn , Paul Rutland , Susan Malcolm , Robin M. Winter & William Reardon