Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: A Chinese case-control study followed by systematic review of existing evidence

Acta Paediatrica, International Journal of Paediatrics

Volumn 100, Issue 7, 2011, Pages 966-971

  Long, Jun ^a   Zhang, Shaofang ^a   Fang, Xiaoyan ^a   Luo, Yuyuan ^a   Liu, Jiebo ^a  

^a Baoan Central Hospital of Shenzhen The Fifth Affiliated Hospital of Shenzhen University   (China)

Author keywords

Case control study; Genetic polymorphisms; Meta analysis; Neonatal hyperbilirubinemia; UDP glucuronosyltransferase 1A1

Indexed keywords

GLUCURONOSYLTRANSFERASE 1A1;

AGAR GEL ELECTROPHORESIS; ARTICLE; ASIAN; BILIRUBIN BLOOD LEVEL; BIRTH WEIGHT; CASE CONTROL STUDY; CHINESE; CONTROLLED STUDY; ETHNICITY; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; GESTATIONAL AGE; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; NEWBORN; NEWBORN JAUNDICE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GLUCURONOSYLTRANSFERASE; HUMANS; HYPERBILIRUBINEMIA, NEONATAL; INFANT, NEWBORN; MALE; MUTATION; RISK FACTORS;

EID: 79958051524     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1111/j.1651-2227.2011.02176.x     Document Type: Article

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