Clinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability

Clin Dysmorphol. 2015 Oct;24(4):151-5. doi: 10.1097/MCD.0000000000000096.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Child
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 12*
  • DNA Copy Number Variations
  • Genetic Association Studies
  • Humans
  • Intellectual Disability / genetics*
  • Male
  • Sequence Deletion