Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder

Eur J Hum Genet. 2013 Apr;21(4):361-5. doi: 10.1038/ejhg.2012.166. Epub 2012 Aug 22.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Apraxias / genetics*
  • Chromosomes, Human, Pair 16 / genetics*
  • Humans
  • Sequence Deletion*