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  • Molecular assay reagents intended to identify gene variants associated with Hirschsprung disease, a disorder characterized by the failure of enteric nerves to develop properly leading to loss of intestinal peristalsis. Genetic variants at multiple loci have been associated with Hirschsprung disease. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Hirschsprung disease-associated loci simultaneously.
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