Author:
Rutland Paul,Pulleyn Louise J.,Reardon William,Baraitser Michael,Hayward Richard,Jones Barry,Malcolm Sue,Winter Robin M.,Oldridge Michael,Slaney Sarah F.,Poole Michael D.,Wilkie Andrew O.M.
Publisher
Springer Science and Business Media LLC
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3. Reardon, W., Winter, R.M., Rutland, P., Pulleyn, L.J., Jones, B.M. & Malcolm, S. Mutations in the fibroblast growth factor 2 gene cause Crouzon syndrome. Nature Genet. 8, 98–103 (1994).
4. Jabs, E.W. et al. Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2. Nature Genet. 8, 275–279 (1994).
5. Wilkie, A.O.M. et al. Apert syndrome results from localised mutations of FGFR2 and is allelic with Crouzon syndrome. Nature Genet. 9, XX–YY (1995).
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