Multiple synostoses syndrome in three members of a family displaying a novel mutation in NOGGIN gene

J Plast Reconstr Aesthet Surg. 2013 Oct;66(10):e287-9. doi: 10.1016/j.bjps.2013.05.011. Epub 2013 Jun 1.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics
  • Adult
  • Carrier Proteins / genetics*
  • Child, Preschool
  • Female
  • Humans
  • Infant
  • Male
  • Mutation*
  • Syndrome
  • Synostosis / genetics*

Substances

  • Carrier Proteins
  • noggin protein