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Preview | Issue Date | Title | Author(s) |
---|---|---|---|
1995 | Apert syndrome results from localised mutations of FGFR2 and is allelic with Crouzon syndrome | Wilkie, A.; Slaney, S.; Oldridge, M.; Poole, M.; Ashworth, G.; Hockley, A.; Hayward, R.; David, D.; Pulleyn, L.; Rutland, P.; Malcolm, S.; Winter, R.; Reardon, W. |
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- 1 1995