Underestimation of the contribution of 211 G to A variation in UGT1A1 to neonatal hyperbilirubinemia in China
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference10 articles.
1. Clinical and genetic etiologies of neonatal unconjugated hyperbilirubinemia in the China Neonatal Genomes Project;Mei;J Pediatr,2022
2. Clinical significance of UGT1A1 genetic analysis in Chinese neonates with severe hyperbilirubinemia;Yang;Pediatr Neonatol,2016
3. Relationship between bilirubin UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia;Huang;Pediatr Res,2002
4. Effect of UDP-glucuronosyltransferase 1A1 activity on risk for developing Gilbert's syndrome;Huang;Kaohsiung J Med Sci,2019
5. 211 G to a variation of UDP-glucuronosyl transferase 1A1 gene and neonatal breastfeeding jaundice;Chou;Pediatr Res,2011
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1. Etiology analysis for term newborns with severe hyperbilirubinemia in eastern Guangdong of China;World Journal of Clinical Cases;2023-04-16
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