ROR2 is mutated in hereditary brachydactyly with nail dysplasia, but not in Sorsby syndrome

Clin Genet. 2003 Sep;64(3):263-5. doi: 10.1034/j.1399-0004.2003.00139.x.
No abstract available

Publication types

  • Comparative Study
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Coloboma / genetics
  • Female
  • Fingers / abnormalities
  • Foot Deformities, Congenital / genetics
  • Genes, Dominant
  • Humans
  • Limb Deformities, Congenital / genetics*
  • Macula Lutea / abnormalities
  • Male
  • Nails, Malformed*
  • Nose / abnormalities
  • Pedigree
  • Receptor Tyrosine Kinase-like Orphan Receptors
  • Receptors, Cell Surface / genetics*
  • Receptors, Cell Surface / physiology
  • Syndrome
  • Tooth Abnormalities / genetics
  • Wales

Substances

  • Receptors, Cell Surface
  • ROR2 protein, human
  • Receptor Tyrosine Kinase-like Orphan Receptors

Associated data

  • OMIM/113000
  • OMIM/120400
  • OMIM/268310