Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: a Chinese case-control study followed by systematic review of existing evidence
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2011.02176.x/fullpdf
Reference29 articles.
1. Early recognition of neonatal hyperbilirubinemia and its emergent management;Smitherman;Semin Fetal Neonatal Med,2006
2. Risk management of severe neonatal hyperbilirubinemia to prevent kernicterus;Bhutani;Clin Perinatol,2005
3. Pharmacogenomics of human UDP-glucuronosyltransferase enzymes;Guillemette;Pharmacogenomics J,2003
4. Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism;Maruo;Pediatrics,1999
5. Exploring the genetic architecture of neonatal hyperbilirubinemia;Watchko;Semin Fetal Neonatal Med,2010
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