Partial deletion of the short arm of chromosome 3: further delineation of the 3p25-3pter syndrome

Clin Genet. 1986 Aug;30(2):127-30. doi: 10.1111/j.1399-0004.1986.tb00581.x.

Abstract

A male newborn with partial deletion of the short arm of chromosome 3 is described. The patient shares most of the features with the previously reported cases. In addition, cardiac, skeletal and gastrointestinal anomalies not previously reported are described. These characteristics may help in further delineation of the syndrome.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 3*
  • Humans
  • Infant, Newborn
  • Male
  • Syndrome