A (14;20) translocation, unbalanced, from a subject with severe congenital anomalies. Respository identification No. GM-981

Cytogenet Cell Genet. 1978;21(3):173. doi: 10.1159/000130891.
No abstract available

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Child, Preschool
  • Chromosomes, Human, 13-15*
  • Chromosomes, Human, 19-20*
  • Female
  • Humans
  • Translocation, Genetic*