Showing results (11-20 of 12) with videos related to
Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 12 results.
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.Pageof 2