A new centromeric heteromorphism in the short arm of chromosome 20

J Med Genet. 1988 Sep;25(9):636-7. doi: 10.1136/jmg.25.9.636.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / genetics
  • Centromere / ultrastructure
  • Chromosomes, Human, Pair 20 / ultrastructure*
  • Female
  • Heterochromatin / ultrastructure*
  • Humans
  • Infant, Newborn
  • Phenotype
  • Polymorphism, Genetic*

Substances

  • Heterochromatin