A family with a presumptive C-F translocation in five generations

Ann Genet. 1971 Mar;14(1):13-21.
No abstract available

MeSH terms

  • Abnormalities, Multiple
  • Adolescent
  • Adult
  • Birth Weight
  • Child, Preschool
  • Chromosome Aberrations* / genetics*
  • Chromosome Disorders*
  • Chromosomes, Human, 19-20*
  • Chromosomes, Human, 6-12 and X*
  • Dermatoglyphics
  • Face / abnormalities
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Intellectual Disability
  • Karyotyping
  • Male
  • Pedigree