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  • Molecular assay reagents intended to identify gene variants associated with Waardenburg syndrome, a collection of genetic diseases characterized by hearing loss and abnormal pigmentation of the eyes, hair, and skin. Genetic variants at multiple loci have been associated with Waardenburg syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Waardenburg syndrome-associated loci simultaneously.
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