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  • Molecular assay reagents intended to identify genetic variants associated with Alagille syndrome, a multisystem disorder affecting the liver, heart, and other parts of the body. Genetic variants at multiple loci have been associated with Alagille syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Alagille syndrome-associated loci simultaneously.
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