Brachydactyly type B1: report of a family with de novo ROR2 mutation

Clin Genet. 2006 Dec;70(6):538-40. doi: 10.1111/j.1399-0004.2006.00719.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Foot Deformities, Congenital / diagnostic imaging
  • Foot Deformities, Congenital / genetics*
  • Hand Deformities, Congenital / diagnostic imaging
  • Hand Deformities, Congenital / genetics*
  • Humans
  • Jordan
  • Male
  • Mutation / genetics*
  • Phenotype*
  • Radiography
  • Receptor Tyrosine Kinase-like Orphan Receptors
  • Receptors, Cell Surface / genetics*

Substances

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