Molecular Analysis of Twist1 and FGF Receptors in a Rabbit Model of Craniosynostosis: Likely Exclusion as the Loci of Origin
Figure 1
No structural mutations in FGFR3 in CS rabbits. Schematic depiction of FGFR3, with locations of primers employed. Full-length rabbit clones for FGFR3 were 3684 bp, as compared to approximately 4300 bp in human FGFR3.
