Gary A. Bellus

A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

I. Kaitila, A. Aylsworth, G. Bellus, 1995, Nature Genetics.

Hypochondroplasia: Molecular Analysis of the Fibroblast Growth Factor Receptor 3 Gene

I. Kaitila, A. Aylsworth, G. Bellus, 1996, Annals of the New York Academy of Sciences.