Xq12-q13.3 duplication: evidence of a recurrent syndrome

Ann Neurol. 2012 Nov;72(5):821-2; author reply 822-3. doi: 10.1002/ana.23754.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Child Development Disorders, Pervasive / genetics*
  • Chromosomes, Human, X / genetics*
  • Developmental Disabilities / genetics*
  • Female
  • Genetic Diseases, X-Linked / genetics*
  • Humans
  • Male