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  • Molecular assay reagents intended to identify gene variants associated with Pendred syndrome, a genetic disorder associated with hearing loss and goiter (i.e., thyroid enlargement). Genetic variants at multiple loci have been associated with Pendred syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Pendred syndrome-associated loci simultaneously.
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