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

Gelijkaardige items

• Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2
  door: Rapley, E A, et al.
  Gepubliceerd in: (2000)
• Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour
  door: Scott, R H, et al.
  Gepubliceerd in: (2006)
• Correlation between a specific Wilms tumour suppressor gene (WT1) mutation and the histological findings in Wilms tumour (WT)
  door: Shibata, R, et al.
  Gepubliceerd in: (2002)
• Controversies and advances in the management of Wilms' tumour
  door: Pritchard-Jones, K
  Gepubliceerd in: (2002)
• Wilms’ Tumour gene 1 (WT1) as an immunotherapeutic target
  door: Coosemans, A.
  Gepubliceerd in: (2011)