Fibroblast growth factors genetics

Bellus GA, McIntosh I, Smith EA, Aylsworth AS, Kaitila I, Horton WA, et al. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia. Nat Genet 1995 10 357-9. 

Colvin JS, Bohne BA, Harding GW, McEwen DG, Ornitz DM. Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3, Nat Genet 1996 12 390-7. 

Tavormina P, Shiang R, Thompson L, Zhu Y, Wilkin D, Lachman R, et al. Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3. Nat Genet 1995 9 321-8. 

Bellus GA, Mack ML, et al. Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome. Am J Hmn Genet 1998 63 711-6. 

Michelson, A.M., Gisselbrecht, S., Zhou, Y., Back, K.H., and Buff, E.M. (1998b). Dual functions of the heartless fibroblast growth factor receptor in development of the Drosophila embryonic mesoderm. Dev. Genet. 22 212-229. 

R. M. Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locus. Eur. J. Hum. Genet, 4, 283-291 (1996)... 

S. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome. Nat. Genet, 8, 98-103 (1994)... 

Meyers, G.A. Orlow, S.J. Munro, I.R. Przylepa, K.A. Jabs, E.W. Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crou-zon syndrome with acanthosis nigricans. Nat. Genet., 11, 462-464 (1995)... 

Mizuno, K. et al.. Effect of chitosan film containing basic fibroblast growth factor on wound healing in genetically diabetic mice, J. Biomed. Mater. Res., 64A, 177,2003. 

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