A case of 10p- syndrome

Ann Genet. 1983;26(2):109-11.

Abstract

A new case with partial deletion of the short arm of one chromosome 10 and multiple malformations is reported.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Deletion
  • Chromosomes, Human, 6-12 and X / ultrastructure*
  • Humans
  • Infant
  • Karyotyping
  • Male
  • Syndrome