Deletion of the short arm of chromosome 2 from a subject with congenital anomalies. Repository identification no. GM-1138

Cytogenet Cell Genet. 1977;18(2):108. doi: 10.1159/000130755.
No abstract available

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Aberrations*
  • Chromosome Deletion*
  • Chromosomes, Human, 1-3*
  • Humans
  • Infant, Newborn
  • Male