A new mutation in the gene ROR2 causes brachydactyly type B1

Purified Wnt5a Protein Activates or Inhibits β-Catenin–TCF Signaling Depending on Receptor Context

Amanda Mikels, Roel Nusse · PLoS Biology · 2006 · 1.3K citations · Full text

Life Sciences, Cell Biology, Molecular Biology +14

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

Ali R. Afzal, Anna Rajab, Christiane Fenske et al. · Nature Genetics · 2000 · 305 citations

Life Sciences, Genetics, Molecular Genetics +7

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome

Hans van Bokhoven, Jacopo Celli, Hülya Kayserili et al. · Nature Genetics · 2000 · 270 citations

Life Sciences, Genetics, Molecular Genetics +7

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