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

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.
  • 作者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.
  • 卷第10卷
  • 期第3期
  • 印刷ISSN1061-4036
  • 电子ISSN1546-1718
  • 文件大小472.94KB
  • 发表时间1995
  • DOI10.1038/ng0795-357
  • 页码357-359
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