[Phenotype variability in thirteen 16p11.2 deletion patients]

An Pediatr (Engl Ed). 2018 Jul;89(1):62-63. doi: 10.1016/j.anpedi.2017.08.003. Epub 2017 Oct 14.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Adult
  • Autistic Disorder / genetics*
  • Child
  • Chromosome Deletion
  • Chromosome Disorders / genetics*
  • Chromosomes, Human, Pair 16 / genetics
  • Female
  • Humans
  • Intellectual Disability / genetics*
  • Male
  • Phenotype

Supplementary concepts

  • 16p11.2 Deletion Syndrome