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  • Molecular assay reagents intended to identify genetic variants associated with Bardet-Biedl syndrome, a multisystem disorder characterized by vision loss, obesity, and additional signs and symptoms affecting other parts of the body. Genetic variants at multiple loci have been associated with Bardet-Biedl syndrome. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Bardet-Biedl syndrome-associated loci simultaneously.
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