Familial transmission of a chromosomal translocation t(2q+;Cp-)

J Med Genet. 1969 Jun;6(2):174-9. doi: 10.1136/jmg.6.2.174.
No abstract available

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adult
  • Chromosome Aberrations*
  • Chromosome Disorders*
  • Chromosomes, Human, 1-3*
  • Chromosomes, Human, 6-12 and X*
  • Cytogenetics
  • Female
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Male