Clinical spectrum of fibroblast growth f
β
M.R. Passos-Bueno; W.R. Wilcox; E.W. Jabs; A.L. SertiΓ©; L.G. Alonso; H. Kitoh
π
Article
π
1999
π
John Wiley and Sons
π
English
β 287 KB
π 1 views
During the last few years, it has been demonstrated that some syndromic craniosynostosis and short-limb dwarfism syndromes, a heterogeneous group comprising of 11 distinct clinical entities, are caused by mutations in one of three fibroblast growth factor receptor genes (FGFR1, FGFR2, and FGFR3). Th