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  • Molecular assay reagents intended to identify gene variants associated with syndromic hearing loss and deafness, a collection of genetic hearing loss and deafness diseases that occur in parallel with signs and symptoms of syndromes affecting other parts of the body. Genetic variants at multiple loci have been associated with syndromic hearing loss and deafness. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple syndromic hearing loss and deafness-associated loci simultaneously.
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