Constitutional WT1 mutations correlate with clinical features in children with progressive nephropathy

Documenti analoghi

• Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?
  di: Kikuchi, H, et al.
  Pubblicazione: (1998)
• Familial Wilms tumour resulting from WT1 mutation: intronic polymorphism causing artefactual constitutional homozygosity
  di: PRITCHARD-JONES, K., et al.
  Pubblicazione: (2000)
• Genomic changes in the WT-gene (WT1) in Wilms' tumors and their correlation with histology.
  di: Kikuchi, H., et al.
  Pubblicazione: (1992)
• A necropsy case of Denys-Drash syndrome with a WT1 mutation in exon 7
  di: Fukuzawa, R, et al.
  Pubblicazione: (2002)
• Correlation between a specific Wilms tumour suppressor gene (WT1) mutation and the histological findings in Wilms tumour (WT)
  di: Shibata, R, et al.
  Pubblicazione: (2002)