The relationship between Gly71Arg and TATA box polymorphism of UGT1A1 gene and prolonged hyperbilirubinemia of breast milk feeding infant in Korean
Author:
Affiliation:
1. Department of Pediatrics, Sung-Ae General Hospital, Seoul, Korea.
Publisher
Korean Pediatric Society
Subject
Pediatrics,Pediatrics, Perinatology, and Child Health
Reference35 articles.
1. Prolonged Neonatal Unconjugated Hyperbilirubinemia Associated with Breast Feeding and a Steroid, Pregnane-3 (Alpha), 20 (Beta)-Diol, in Maternal Milk That Inhibits Glucuronide Formation In Vitro*
2. Breast mild jaundice: Natural history, familial incidence and late neurodevelopmental outcome of the infant
3. The genetic basis of Gilbert's syndrome
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Should We Consider UGT1A1 Mutation Analysis in Evaluating the Prolonged Jaundice of Newborn Infants?;Neonatal Medicine;2024-02-29
2. A case of concomitant Gilbert's syndrome and hereditary spherocytosis;The Korean Journal of Hepatology;2010
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