Familial Wilms tumour resulting from WT1 mutation: intronic polymorphism causing artefactual constitutional homozygosity

J Med Genet. 2000 May;37(5):377-9. doi: 10.1136/jmg.37.5.377.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Amino Acid Sequence
  • DNA-Binding Proteins / genetics*
  • Female
  • Genes, Wilms Tumor*
  • Homozygote
  • Humans
  • Introns / genetics
  • Male
  • Molecular Sequence Data
  • Mutation
  • Pedigree
  • Transcription Factors / genetics*
  • WT1 Proteins
  • Wilms Tumor / genetics*

Substances

  • DNA-Binding Proteins
  • Transcription Factors
  • WT1 Proteins