[Microdeletion 2q23.1 and syndromic findings]

Rev Neurol. 2013 Nov 1;57(9):430-1.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports
  • English Abstract
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 2 / genetics*
  • Developmental Disabilities / genetics*
  • Epilepsy / genetics*
  • Humans
  • Infant
  • Male
  • Syndrome