A chromosomal abnormality (21q-) in primary thrombocytosis

Hum Genet. 1979;50(1):105-6. doi: 10.1007/BF00295597.

Abstract

A patient with thrombocytosis was found to present an acquired deletion of the long arm of chrosome 21 (21q-). A similar observation reported in the literature is hereby confirmed.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Chromosome Deletion*
  • Chromosomes, Human, 21-22 and Y*
  • Female
  • Humans
  • Thrombocytosis / genetics*