De novo Robertsonian D/D type translocations: the Leuven experience

Clin Genet. 1989 Jul;36(1):65-8. doi: 10.1111/j.1399-0004.1989.tb03368.x.

Abstract

In this paper we report a de novo 13/14 Robertsonian type translocation with apparent loss of band 14q11 in a mentally retarded, blind 24-year-old male. The findings in 10 other patients with a de novo Robertsonian D/D type translocation diagnosed in this center are reviewed.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosomes, Human, Pair 13*
  • Chromosomes, Human, Pair 14*
  • Humans
  • Intellectual Disability / genetics
  • Karyotyping
  • Male
  • Syndrome
  • Translocation, Genetic*