A further patient with Noonan syndrome due to a SOS1 mutation and rhabdomyosarcoma

Genes Chromosomes Cancer. 2010 Oct;49(10):967-8. doi: 10.1002/gcc.20800.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Female
  • Humans
  • Infant, Newborn
  • Mutation, Missense / genetics*
  • Noonan Syndrome / genetics*
  • Noonan Syndrome / pathology
  • Prognosis
  • Rhabdomyosarcoma / genetics*
  • SOS1 Protein / genetics*

Substances

  • SOS1 Protein