The t(8;13) atypical myeloproliferative disorder: further analysis of the ZNF198 gene and lack of evidence for multiple genes disrupted on chromosome 13

Blood. 1998 Aug 15;92(4):1456-8.
No abstract available

Publication types

  • Comparative Study
  • Letter

MeSH terms

  • Carrier Proteins*
  • Chromosomes, Artificial, Yeast
  • Chromosomes, Human, Pair 13 / genetics
  • Chromosomes, Human, Pair 13 / ultrastructure*
  • Chromosomes, Human, Pair 8 / genetics
  • Chromosomes, Human, Pair 8 / ultrastructure*
  • Cloning, Molecular
  • DNA Mutational Analysis
  • DNA, Complementary / genetics
  • DNA, Neoplasm / genetics
  • DNA-Binding Proteins / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Introns / genetics
  • Myeloproliferative Disorders / genetics*
  • Myeloproliferative Disorders / pathology
  • Neoplasm Proteins / genetics*
  • Receptor Protein-Tyrosine Kinases*
  • Receptor, Fibroblast Growth Factor, Type 1
  • Receptors, Fibroblast Growth Factor / genetics
  • Recombinant Fusion Proteins / analysis
  • Transcription Factors
  • Translocation, Genetic*

Substances

  • Carrier Proteins
  • DNA, Complementary
  • DNA, Neoplasm
  • DNA-Binding Proteins
  • Neoplasm Proteins
  • Receptors, Fibroblast Growth Factor
  • Recombinant Fusion Proteins
  • Transcription Factors
  • ZMYM2 protein, human
  • FGFR1 protein, human
  • Receptor Protein-Tyrosine Kinases
  • Receptor, Fibroblast Growth Factor, Type 1