Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2

A human chondrodysplasia due to a mutation in a TGF-β superfamily member

J. Terrig Thomas, Keming Lin, Maithily Nandedkar et al. · Nature Genetics · 1996 · 417 citations · Full text

Medicine, Genetics, Pathology +13

Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1

Jack Thomas, Michael W. Kilpatrick, Kerning Lin et al. · Nature Genetics · 1997 · 358 citations

Life Sciences, Developmental Biology, Genetics +14

A novel family of cell surface receptors with tyrosine kinase-like domain.

Piotr Masiakowski, R.D. Carroll · Journal of Biological Chemistry · 1992 · 273 citations · Full text

Life Sciences, Developmental Biology, Molecular Biology +12

Ror2, encoding a receptor-like tyrosine kinase, is required for cartilage and growth plate development

Thomas M. DeChiara, Robert B. Kimble, William Poueymirou et al. · Nature Genetics · 2000 · 254 citations

Life Sciences, Developmental Biology, Molecular Biology +13

Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B

Michael Oldridge, Ana María Fortuna, Monika Maringa et al. · Nature Genetics · 2000 · 232 citations

Life Sciences, Genetics, Molecular Genetics +10