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A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
Gary A. Bellus, Iain McIntosh, E. Anne Smith, Arthur S. Aylsworth, Ilkka Kaitila, William A. Horton, Giselle A. Greenhaw, Jacqueline T. Hecht, Clair A. Francomano
Research output: Contribution to journal › Article › peer-review
351
Scopus
citations