A (9;17) translocation, 46 chromosomes. Repository identification No. GM-988

Cytogenet Cell Genet. 1977;18(4):244. doi: 10.1159/000130769.
No abstract available

Publication types

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

MeSH terms

  • Chromosome Aberrations*
  • Chromosomes, Human, 16-18*
  • Chromosomes, Human, 6-12 and X*
  • Humans
  • Infant, Newborn
  • Male
  • Translocation, Genetic*