A 1/G translocation in a member of a kindred with a marker chromosome

Arch Intern Med. 1967 Mar;119(3):297-301.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Chromosome Aberrations / genetics*
  • Chromosome Disorders
  • Dermatoglyphics
  • Female
  • Humans
  • Intellectual Disability*
  • Karyotyping