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

Andrew O.M. Wilkie(University of Oxford), Sarah F. Slaney(Churchill Hospital), Michael Oldridge(John Radcliffe Hospital), Michael D. Poole(University of Oxford), Geraldine J. Ashworth(University of Oxford), Anthony D. Hockley(Queen Elizabeth Hospital Birmingham), Richard Hayward(University College London), David J. David(Women's and Children's Hospital), Louise J. Pulleyn, Paul Rutland, S Malcolm, Robin M. Winter, William Reardon
Nature Genetics
February 1, 1995
Cited by 936

Abstract


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