Deletion of the short arm of chromosome 20

Clin Genet. 1987 Jun;31(6):406-9. doi: 10.1111/j.1399-0004.1987.tb02833.x.

Abstract

A de novo deletion of the short arm of chromosome 20--del (20) (p11) or (p11p13)--is described in a child with psychomotor retardation and multiple congenital anomalies.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 20*
  • Humans
  • Infant
  • Intellectual Disability / genetics*
  • Male