Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

Rita Shiang, Leslie M. Thompson, Yazhen Zhu et al. · Cell · 1994 · 1.3K citations

Life Sciences, Genetics, Molecular Genetics +13

Fibroblast Growth Factor Receptor 3 Is a Negative Regulator of Bone Growth

Anthony Wynshaw‐Boris, Fen Zhou, Ann Kuo et al. · Cell · 1996 · 1.1K citations · Full text

Medicine, Cell Biology, Orthopaedic Surgery +12

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

Andrew O.M. Wilkie, Sarah F. Slaney, Michael Oldridge et al. · Nature Genetics · 1995 · 937 citations

Life Sciences, Genetics, Molecular Genetics +7

Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

Francis Rousseau, Jacky Bonaventure, Laurence Legeai‐Mallet et al. · Nature · 1994 · 934 citations

Life Sciences, Genetics, Molecular Genetics +6

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3

Jennifer S. Colvin, Barbara A. Bohne, Gary W. Harding et al. · Nature Genetics · 1996 · 869 citations

Medicine, Cell Biology, Molecular Genetics +14