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

Lignende værker

• Bilateral Wilms’ tumors in an infant with Denys-Drash syndrome and rarely seen truncation mutation in the WT1 gene-exon 6
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  af: Alge, Joseph L., et al.
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• Correlation between a specific Wilms tumour suppressor gene (WT1) mutation and the histological findings in Wilms tumour (WT)
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