Expanding the phenotypic and genetic spectrum of radioulnar synostosis associated hematological disease

Haematologica. 2018 Jul;103(7):e284-e287. doi: 10.3324/haematol.2017.183855. Epub 2018 Mar 8.
No abstract available

Publication types

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

MeSH terms

  • Female
  • Genetic Association Studies*
  • Genetic Variation*
  • Hematologic Diseases / complications*
  • Hematologic Diseases / diagnosis*
  • Homeodomain Proteins / genetics
  • Humans
  • MDS1 and EVI1 Complex Locus Protein / genetics
  • Male
  • Mutation
  • Pedigree
  • Phenotype*
  • Radius / abnormalities*
  • Radius / diagnostic imaging
  • Synostosis / complications
  • Synostosis / diagnosis*
  • Synostosis / genetics*
  • Ulna / abnormalities*
  • Ulna / diagnostic imaging

Substances

  • HOXA11 protein, human
  • Homeodomain Proteins
  • MDS1 and EVI1 Complex Locus Protein
  • MECOM protein, human

Supplementary concepts

  • Radioulnar Synostosis