https://www.selleckchem.com/pr....oducts/pi3k-hdac-inh
Detection of all major classes of genomic variants in a single test would decrease cost and increase the efficiency of genomic diagnostics. Genome sequencing (GS) has the potential to provide this level of comprehensive detection. We sought to demonstrate the utility of GS in the molecular diagnosis of 18 patients with clinically defined Alagille syndrome (ALGS), who had a negative or inconclusive result by standard-of-care testing. We performed GS on 16 pathogenic variant-negative probands and two probands with inconclusi
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