FGFR3 gene mutations associated with human skeletal disorders occur rarely in multiple myeloma

Blood. 1998 Oct 15;92(8):2987-9.
No abstract available

Publication types

  • Comment
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Amino Acid Substitution
  • Bone Diseases, Developmental / genetics*
  • Cell Transformation, Neoplastic / genetics
  • Chromosomes, Human, Pair 14 / genetics*
  • Chromosomes, Human, Pair 14 / ultrastructure
  • Chromosomes, Human, Pair 4 / genetics*
  • Chromosomes, Human, Pair 4 / ultrastructure
  • DNA, Neoplasm / genetics
  • Humans
  • Multiple Myeloma / genetics*
  • Point Mutation
  • Polymorphism, Single-Stranded Conformational
  • Protein-Tyrosine Kinases*
  • Receptor, Fibroblast Growth Factor, Type 3
  • Receptors, Fibroblast Growth Factor / genetics*
  • Translocation, Genetic*
  • Tumor Cells, Cultured

Substances

  • DNA, Neoplasm
  • Receptors, Fibroblast Growth Factor
  • FGFR3 protein, human
  • Protein-Tyrosine Kinases
  • Receptor, Fibroblast Growth Factor, Type 3