A fourth case of BCR-FGFR1 positive CML-like disease with t(8;22) translocation showing an extensive deletion on the derivative chromosome 8p

Hematol J. 2002;3(6):315-6. doi: 10.1038/sj.thj.6200201.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Aged
  • Chromosome Deletion
  • Chromosomes, Human, Pair 22
  • Chromosomes, Human, Pair 8
  • Diagnosis, Differential
  • Female
  • Gene Rearrangement
  • Humans
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / diagnosis
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics*
  • Myeloproliferative Disorders / diagnosis
  • Myeloproliferative Disorders / genetics*
  • Oncogene Proteins / genetics*
  • Oncogene Proteins, Fusion
  • Protein-Tyrosine Kinases*
  • Proto-Oncogene Proteins c-bcr
  • Proto-Oncogene Proteins*
  • Receptor Protein-Tyrosine Kinases / genetics*
  • Receptor, Fibroblast Growth Factor, Type 1
  • Receptors, Fibroblast Growth Factor / genetics*
  • Translocation, Genetic*

Substances

  • Oncogene Proteins
  • Oncogene Proteins, Fusion
  • Proto-Oncogene Proteins
  • Receptors, Fibroblast Growth Factor
  • FGFR1 protein, human
  • Protein-Tyrosine Kinases
  • Receptor Protein-Tyrosine Kinases
  • Receptor, Fibroblast Growth Factor, Type 1
  • BCR protein, human
  • Proto-Oncogene Proteins c-bcr