William A. Horton

International nosology of heritable disorders of connective tissue, Berlin, 1986

Peter Beighton, A. De Paepe, D. M. Danks et al. · American Journal of Medical Genetics · 1988 · 729 citations

Gross Anatomy, Mendelian Disorder, Histopathology +6

Achondroplasia is defined by recurrent G380R mutations of FGFR3.

Gary A. Bellus, Timothy Hefferon, Rosa Isela Ortiz De Luna et al. · PubMed · 1995 · 482 citations

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

Gary A. Bellus, Iain McIntosh, Elizabeth A. Smith et al. · Nature Genetics · 1995 · 475 citations

Recurrent Mutation, Signal Transduction, Bone Morphogenic Protein +8

Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)

Jung Ahn, Hermann‐Josef Lüdecke, Steffi Lindow et al. · Nature Genetics · 1995 · 428 citations

Genetics, Pathology, Molecular Genetics +6

Effect of IGF-I in the Chondrogenesis of Bone Marrow Mesenchymal Stem Cells in the Presence or Absence of TGF-β Signaling

Lara Longobardi, Lynda O’Rear, Srikanth Aakula et al. · Journal of Bone and Mineral Research · 2006 · 341 citations