Human telomeric 6; 19 translocation chromosome with a tendency to break at the fusion point

Chromosoma. 1983;88(2):139-44. doi: 10.1007/BF00327334.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics
  • Chromosomes, Human, 19-20* / ultrastructure
  • Chromosomes, Human, 6-12 and X* / ultrastructure
  • Female
  • Humans
  • Intellectual Disability / genetics
  • Lymphocytes / ultrastructure
  • Models, Genetic
  • Translocation, Genetic*