A 13;13 tandem chromosome translocation in a subject with congenital anomalies. Repository identification No. GM-2018

Cytogenet Cell Genet. 1979;24(1):72. doi: 10.1159/000131359.
No abstract available

Publication types

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

MeSH terms

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