Partial trisomy of 11 and 22 due to familial translocation t(11;22)(q23;q11), inherited in three generations

Hum Genet. 1979 Oct 2;51(3):349-55. doi: 10.1007/BF00283408.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adult
  • Chromosomes, Human, 21-22 and Y*
  • Chromosomes, Human, 6-12 and X*
  • Dermatoglyphics
  • Female
  • Humans
  • Infant
  • Intellectual Disability / genetics*
  • Karyotyping
  • Male
  • Pedigree
  • Phenotype
  • Sex Chromosomes*
  • Translocation, Genetic*
  • Trisomy*
  • X Chromosome*