Complex t(8;19;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia

Cancer Genet Cytogenet. 2008 Sep;185(2):109-12. doi: 10.1016/j.cancergencyto.2008.05.007.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Chromosomes, Human, Pair 19*
  • Chromosomes, Human, Pair 21*
  • Chromosomes, Human, Pair 8*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Leukemia, Myeloid, Acute / genetics*
  • Male
  • Translocation, Genetic*