[Significance of the type of chromosome aberrations and biochemical disorders for diagnosis of Down's syndrome and the phenotype of partial trisomy 21]

Pediatr Pol. 1980 Jan;55(1):23-32.
[Article in Polish]
No abstract available

Publication types

  • Case Reports
  • Comparative Study
  • English Abstract

MeSH terms

  • Chromosomes, Human, 21-22 and Y*
  • Diagnosis, Differential
  • Down Syndrome / diagnosis*
  • Down Syndrome / genetics
  • Erythrocytes / enzymology
  • Female
  • Humans
  • Infant
  • Karyotyping
  • Phenotype
  • Superoxide Dismutase / blood
  • Translocation, Genetic*
  • Trisomy*

Substances

  • Superoxide Dismutase