A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
Bellus, Gary A., McIntosh, Iain, Smith, E. Anne, Aylsworth, Arthur S., Kaitila, Ilkka, Horton, William A., Greenhaw, Giselle A., Hecht, Jacqueline T., Francomano, Clair A.Volume:
10
Year:
1995
Pages:
3
DOI:
10.1038/ng0795-357
File:
PDF, 473 KB
1995