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  • Molecular assay reagents intended to identify stable and usually irreversible anomalies (e.g., mutations, deletions, trinucleotide repeats) in the genes that may cause disorders in humans; genetic anomalies many be de novo or inherited (familial), frequently in x-linked, autosomal dominant, or recessive form. Genetic anomalies are common in many hereditary disorders and/or associated with tumor development.
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