Familial transmission of 16p trisomy in an infant

Hum Genet. 1989 Jan;81(2):196-8. doi: 10.1007/BF00293904.

Abstract

Based on four reported cases including the present case, 16p trisomic infants have remarkably similar features. These are severe developmental delay, psychomotor retardation, typical facies, and anomalies of extremities.

Publication types

  • Case Reports

MeSH terms

  • Chromosome Banding
  • Chromosomes, Human, Pair 16*
  • Female
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Syndrome
  • Trisomy*