A necropsy case of Denys-Drash syndrome with a WT1 mutation in exon 7

Παρόμοια τεκμήρια

• Bilateral Wilms’ tumors in an infant with Denys-Drash syndrome and rarely seen truncation mutation in the WT1 gene-exon 6
  ανά: Modi, Jayesh, κ.ά.
  Έκδοση: (2015)
• The Denys-Drash syndrome.
  ανά: Mueller, R F
  Έκδοση: (1994)
• A novel WT1 gene mutation in a chinese girl with denys‐drash syndrome
  ανά: Wang, Faliang, κ.ά.
  Έκδοση: (2021)
• Hemolytic uremic syndrome as the presenting manifestation of WT1 mutation and Denys-Drash syndrome: a case report
  ανά: Alge, Joseph L., κ.ά.
  Έκδοση: (2017)
• Correlation between a specific Wilms tumour suppressor gene (WT1) mutation and the histological findings in Wilms tumour (WT)
  ανά: Shibata, R, κ.ά.
  Έκδοση: (2002)