Two Children with macrocephaly, developmental delay, and PTEN mutation

Clin Pediatr (Phila). 2009 Jan;48(1):89-92. doi: 10.1177/0009922808321679. Epub 2008 Jul 14.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Developmental Disabilities / complications
  • Hamartoma Syndrome, Multiple*
  • Head / abnormalities
  • Humans
  • Membrane Proteins / genetics
  • PTEN Phosphohydrolase / genetics

Substances

  • Membrane Proteins
  • TPTE protein, human
  • PTEN Phosphohydrolase