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  • Molecular assay reagents intended to identify deletions and duplications in genes associated with hypohidrotic ectodermal dysplasias, forms of ectodermal dysplasia characterized by reduced ability to perspire. Genetic variants at multiple loci have been associated with hypohidrotic ectodermal dysplasias. These reagents are intended to detect deletions and duplications in multiple hypohidrotic ectodermal dysplasia-associated loci simultaneously.
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