der(1)t(1;19)(p12;p11): a new nonrandom chromosomal abnormality in myelodysplastic syndrome

Cancer Genet Cytogenet. 1997 Apr;94(2):85-7. doi: 10.1016/s0165-4608(96)00188-4.

Abstract

The der(1)t(1;19)(p12;p11) has not been previously reported in myelodysplastic syndrome (MDS). Fluorescence in situ hybridization (FISH) using chromosome 1- and chromosome 19-specific probes, performed on the bone marrow (BM) cells of this patient confirmed the initial karyotype, i.e., 47,XY,+der(1)t(1;19)(p12;p11).

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosome Aberrations / genetics*
  • Chromosome Banding
  • Chromosome Disorders
  • Chromosomes, Human, Pair 1
  • Chromosomes, Human, Pair 19
  • Humans
  • Male
  • Myelodysplastic Syndromes / genetics*
  • Translocation, Genetic