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  • Molecular assay reagents intended to identify deletions and duplications in genes associated with nonsyndromic hearing loss/deafness, a collection of genetic hearing loss/deafness diseases that are not associated with signs and symptoms affecting other parts of the body. Genetic variants at multiple loci have been associated with nonsyndromic hearing loss/deafness. These reagents are intended to detect deletions and duplications in multiple nonsyndromic hearing loss/deafness-associated loci simultaneously.
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