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

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review