A t(4;9)(q34;p22) translocation associated with partial epilepsy, mental retardation, and dysmorphism

Epilepsia. 2005 Aug;46(8):1322-4. doi: 10.1111/j.1528-1167.2005.64304.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Child
  • Chromosomes, Human, Pair 4*
  • Chromosomes, Human, Pair 9*
  • Epilepsies, Partial / diagnosis
  • Epilepsies, Partial / genetics*
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Intellectual Disability / diagnosis
  • Intellectual Disability / genetics*
  • Neurologic Examination
  • Nuclear Proteins / genetics
  • Phenotype
  • Translocation, Genetic*

Substances

  • MLLT3 protein, human
  • Nuclear Proteins