Expanding the clinical spectrum of MYCN-related Feingold syndrome

Am J Med Genet A. 2006 Oct 15;140(20):2254-6. doi: 10.1002/ajmg.a.31407.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / pathology
  • Child, Preschool
  • Codon, Nonsense / genetics*
  • Humans
  • Limb Deformities, Congenital / genetics*
  • Limb Deformities, Congenital / pathology
  • Male
  • Microcephaly / genetics*
  • Microcephaly / pathology
  • N-Myc Proto-Oncogene Protein
  • Nuclear Proteins / genetics*
  • Oncogene Proteins / genetics*
  • Syndrome

Substances

  • Codon, Nonsense
  • MYCN protein, human
  • N-Myc Proto-Oncogene Protein
  • Nuclear Proteins
  • Oncogene Proteins