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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