Familial insertional translocation

Lancet. 1972 Jul 29;2(7770):231. doi: 10.1016/s0140-6736(72)91668-6.
No abstract available

MeSH terms

  • Abnormalities, Multiple / genetics
  • Child
  • Chromosome Aberrations* / genetics*
  • Chromosome Disorders*
  • Humans
  • Karyotyping