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4. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome;Reardon, W.; Winter, R.M.; Rutland, P.; Pulleyn, U.; Jones, B.M.; Malcolm, S.;Nature Genet,1994
5. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome;Wilkie, A.O.M.; Slaney, S.F.; Oldridge, M.;Nature Genet,1995