Demonstration of uniparental-isodisomy on chromosome 22q11.2 in a patient with childhood schizophrenia and facial dysmorphology by whole-genome analysis

J Neuropsychiatry Clin Neurosci. 2012 Winter;24(1):E13-4. doi: 10.1176/appi.neuropsych.11010027.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Chromosomes, Human, Pair 21 / genetics
  • Facial Asymmetry / complications
  • Facial Asymmetry / genetics*
  • Female
  • Genome
  • Humans
  • Microsatellite Repeats
  • Mosaicism
  • Schizophrenia / complications
  • Schizophrenia / genetics*
  • Trisomy / genetics*
  • Trisomy / physiopathology
  • Uniparental Disomy / genetics*
  • Uniparental Disomy / physiopathology

Supplementary concepts

  • Chromosome 21, uniparental disomy of