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Molecular assay reagents intended to identify gene variants associated with Marfan syndrome, a connective tissue disorder characterized by cardiovascular, eye, and skeletal abnormalities. Genetic variants at multiple loci have been associated Marfan syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Marfan syndrome-associated loci simultaneously.
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