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  • Molecular assay reagents intended to identify deletions or duplications of the Wilms tumor 1 (WT1) gene, located at chromosome 11p13, which encodes the Wilms tumor protein. Genetic variants at this locus have been associated with aniridia, diffuse mesangial sclerosis, Drash syndrome, Frasier syndrome, Meacham syndrome, mesothelioma, and Wilms tumor.
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