Monosomy 10qter: a new case

J Med Genet. 1992 May;29(5):342-3. doi: 10.1136/jmg.29.5.342.

Abstract

A new case of terminal deletion 10q26-qter is described. The phenotypic features are compatible with those of the previously reported cases. Deafness is reported for the first time.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adult
  • Aneuploidy*
  • Chromosome Banding
  • Chromosome Deletion
  • Chromosomes, Human, Pair 10*
  • Humans
  • Infant
  • Infant, Newborn
  • Male