3 results for author:"Poole M.D." in Literature citations
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| Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes. Rutland P., Pulleyn L.J., Reardon W., Baraister M., Hayward R., Jones B.M., Malcolm S., Winter R.M., Oldridge M., Slaney S.F. et al. Nat. Genet. 9:173-176(1995) · UniProtKB (1) |
| Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Wilkie A.O.M., Slaney S.F., Oldridge M., Poole M.D., Ashworth G.J., Hockley A.D., Hayward R.D., David D.J., Pulleyn L.J., Rutland P. et al. Nat. Genet. 9:165-172(1995) · UniProtKB (1) |
| 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., Poole M.D., Pulleyn L.J., Rutland P., Hockley A.D., Wake M.J.C., Goldin J.H., Winter R.M. et al. Hum. Mol. Genet. 4:1077-1082(1995) · UniProtKB (1) |