A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia. - Bellus,G.A.; McIntosh,I.; Smith,E.A.; Aylsworth,A.S.; Kaitila,I.; Horton,W.A.; Greenhaw,G.A.; Hecht,J.T.; Francomano,C.A. (Nat Genet, 1995)