Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
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W. Reardon | D. David | R. Winter | A. Wilkie | M. Poole | S. Malcolm | A. Hockley | R. Hayward | S. Slaney | P. Rutland | L. Pulleyn | M. Oldridge | G. Ashworth