A double translocation culture t(5;15)t(9;11) with partial deletion of the short arm of chromosome 5. Repository identification No. GM-344

Cytogenet Cell Genet. 1975;15(6):400-1. doi: 10.1159/000130539.
No abstract available

Publication types

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

MeSH terms

  • Child
  • Chromosome Aberrations*
  • Chromosome Deletion*
  • Chromosomes, Human, 4-5*
  • Cri-du-Chat Syndrome / genetics*
  • Humans
  • Male
  • Translocation, Genetic*