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新生儿76例ABO溶血临床分析 被引量:1

Clinical Analysis of 76 Cases of Newborns ABO Hemolysis
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作者 侯玉华
出处 《职业与健康》 CAS 2008年第11期1109-1110,共2页 Occupation and Health
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  • 2Monagham G,Ryan M,Seddon R,et al.Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gibert′s syndrome[J].Lancet,1996,347:578-581. 被引量:1
  • 3Beutler E, Gelbart T, Demina A. Racial variability in the UDP-glucuronosyltransferase1(UGTIAI) promoter:a balanced polymorphism for regulation of bilirubin metabolism[J].Proc Natl Acad Sci USA,1998,95:8170-8174. 被引量:1
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  • 7Sugatani J,Yamakawa K,Yoshinari K,et al.Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia[J].Biochemi Biophysical Res Commun,2002,292:492-497. 被引量:1
  • 8Ciotti M,Chen F,Rubaltelli FF,et al. Coding defect and a TATA box mutation at the bilirubin UDP-glucuronotyltransferase gene caude Crigler-Najjar type I disease[J].Biochim Biophy Acta,1998,1407:40-50. 被引量:1
  • 9Sappal BS,Ghosh SS.A novel intronic mutation results in the use of a cryptic splice acceptor site within the coding region of UGTIAI,causing crigler-najjar syndrome type 1[J].Molecu Genet Metabol,2002,75:134-142. 被引量:1
  • 10Yamamoto K,Sato H,Fujiyama Y,et al.Contribution of two missense mutations(G71R and Y486D) of the bilirubin UDP glycosyltransferase(UGT1A1) gene to phenotypes of Gilbert′s syndrome and Crigler-Najjiar syndrome type Ⅱ[J].Biochim Biophys Acta,1998,1406:267-273. 被引量:1

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