A novel t(7;17)(q11;q11) as the sole karyotypic abnormality in childhood pre-B-cell acute lymphoblastic leukemia

Cancer Genet Cytogenet. 1998 Jul 1;104(1):70-1. doi: 10.1016/s0165-4608(97)00393-2.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Chromosome Aberrations / genetics*
  • Chromosome Disorders
  • Chromosomes, Human, Pair 17 / genetics*
  • Chromosomes, Human, Pair 7 / genetics*
  • Humans
  • Karyotyping
  • Male
  • Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Translocation, Genetic / genetics*