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  • Molecular assay reagents intended to identify gene variants associated with multiple lentigines syndrome, a form of rasopathy characterized by brown skin spots, cardiac defects, widely spaced eyes, sunken or protruding chest, and short stature. Genetic variants at multiple loci have been associated with multiple lentigines syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in more than one multiple lentigines syndrome-associated loci simultaneously.
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