[Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)]

Humangenetik. 1973;18(4):321-7. doi: 10.1007/BF00291129.
[Article in French]
No abstract available

MeSH terms

  • Abnormalities, Multiple / genetics
  • Chromosomes, Human, 6-12 and X*
  • Eye Abnormalities
  • Female
  • Growth Disorders / genetics
  • Heart Defects, Congenital / genetics
  • Humans
  • Infant
  • Intellectual Disability / genetics
  • Karyotyping
  • Micrognathism / genetics
  • Palate / abnormalities
  • Pedigree
  • Trisomy*