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Increasing number of screening tests is based on human DNA analysis. Diseases yet of unknown etiology prove to have an underlying genetic factor. Understanding of human genome allows improved diagnosis, better choice of farmacotherapy or more adequate lifestyle modifications. Neonate hyperbilirubinemia has been linked to UGT1A1 gene polymorphism. UGT1A1 gene encodes UDP-glucuronosyltransferase, an...
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