Occurrence of 19p- in an infant with multiple dysmorphic features

Ann Genet. 1984;27(1):56-7.

Abstract

A case with partial deletion on the short arm of one chromosome 19 and multiple dysmorphic features is reported.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / pathology
  • Chromosome Deletion*
  • Chromosomes, Human, 19-20 / ultrastructure*
  • Dermatoglyphics
  • Humans
  • Infant
  • Karyotyping
  • Male