![CDATA[ [if IE 9] ]]>
Atazanavir, Belinostat, GNT1, Irinotecan, Irinotecan glucuronidation, Irinotecan metabolism, Nilotinib, Pazopanib, Phenol/Bilirubin, UDP-Glucuronosyltransferase, UDP-Glucosyltransferase 1, UGT1A1, Uracil Glucuronyl transferase, Uridine Diphosphate Glucosyltransferase 1, Crigler-Najjar Syndrome, Gilbert Syndrome, Hyperbilirubinemia
This is a full gene sequencing test for UGT1A1 that includes the TA repeat region of the promoter and all intron/exon boundaries. Results are interpreted for the purposes of UGT1A1 drug metabolism and hereditary hyperbilirubinemia syndromes (Gilbert syndrome and Crigler-Najjar syndrome).
Urate, Histology, Crystals, Surgical
Ureaplasma urealyticum, Ureaplasma parvum, PCR
RUA and reflex Culture with Susceptibility if the following criteria is present:
Stone Analysis, Kidney, Kidney Stone Risk, U URORKSO