Variant t(1;15;17)(q23;q22;q23) in a case of acute promyelocytic leukemia

Leukemia. 1996 Oct;10(10):1658-61.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosomes, Human, Pair 1*
  • Chromosomes, Human, Pair 15*
  • Chromosomes, Human, Pair 17*
  • Humans
  • Leukemia, Promyelocytic, Acute / genetics*
  • Male
  • Translocation, Genetic*