Partial deletion of ANKRD11 results in the KBG phenotype distinct from the 16q24.3 microdeletion syndrome

  • Mohamed Khalifa
  • , Jennifer Stein
  • , Lance Grau
  • , Valery Nelson
  • , Jeanne Meck
  • , Swaroop Aradhya
  • , John Duby

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)835-840
Number of pages6
JournalAmerican Journal of Medical Genetics, Part A
Volume161
Issue number4
DOIs
StatePublished - Apr 2013
Externally publishedYes

ASJC Scopus Subject Areas

  • Genetics
  • Genetics(clinical)

Keywords

  • 16q24.3
  • ANKRD11
  • ASD
  • Autism
  • KBG
  • MCA/MR
  • Macrodontia
  • Microdeletion
  • Mosaicism

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