Twenty-four new cases ofWT1 germline mutations and review of the literature: Genotype/phenotype correlations for Wilms tumor development
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference58 articles.
1. A point mutation found in the WT1 gene in a sporadic Wilms' tumor without genitourinary abnormalities is identical with the most frequent point mutation in Denys-Drash syndrome
2. Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome
3. The same mutation affecting the splicing ofWT1 gene is present on Frasier syndrome patients with or without Wilms' tumor
4. WT1 Mutations Associated with Incomplete Denys-Drash Syndrome Define a Domain Predicted to Behave in a Dominant-Negative Fashion
5. Nephrogenic rests and the pathogenesis of Wilms tumor: Developmental and clinical considerations
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