1. Sm'ith's recognizable patterns of human nmalfornmation;Jones, K.L.,1988
2. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome;Reardon, W.; Winter, R.M.; Rutland, P.;Nat Genet,1994
3. Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor 2 gene in Crouzon syndrome;Oldridge, M.; Wilkie, A.O.M.; Slaney, S.F.;Hum Mol Genet,1995
4. Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome;Gorry, M.C.; Preston, R.A.; White, G.J.;Hum Mol Genet,1995
5. FGFR2 exon IIIa and IIlc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: a deletion deuveidetoncealftoerrnmaitisvseenRseNAchasnpgleisc;Meyers, G.A.; Day, D.; Goldberg, R.,1996