Inherited deletion of chromosome (21p-) in a child with congenital malformation and psychomotor retardation

Indian Pediatr. 1992 Jul;29(7):929-34.
No abstract available

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Banding
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 21*
  • Humans
  • Infant
  • Intellectual Disability / genetics*
  • Karyotyping
  • Male
  • Pedigree