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Nature Genetics|February 1, 1995
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndromeA O Wilkie, S F Slaney, M Oldridge, et al.Journal of Medical Genetics|August 1, 1997
Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosisW Reardon, D Wilkes, P Rutland, et al.Nature Genetics|September 6, 2000
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C geneM Bitner-Glindzicz, K J Lindley, P Rutland, et al.Pageof 3