Literature DB >> 28927582

211 G to A variation of UGT1A1 and severe neonatal hyperbilirubinemia.

Yu-Jung Lin1, Po-Nien Tsao2.   

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Year:  2017        PMID： 28927582     DOI： 10.1016/j.pedneo.2017.01.008

Source DB:  PubMed          Journal:  Pediatr Neonatol        ISSN： 1875-9572            Impact factor:   2.083


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  2 in total

1.  Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study.

Authors:  Jinfu Zhou; Changyi Yang; Wenbin Zhu; Shuwei Chen; Yinglin Zeng; Jing Wang; Hong Zhao; Yao Chen; Feng Lin
Journal:  Biomed Res Int       Date:  2018-09-12       Impact factor: 3.411

2.  UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China.

Authors:  Hui Yang; Fen Lin; Zi-Kai Chen; Lin Zhang; Jia-Xin Xu; Yong-Hao Wu; Jing-Ying Gu; Yu-Bin Ma; Jian-Dong Li; Li-Ye Yang
Journal:  BMC Pediatr       Date:  2021-06-01       Impact factor: 2.125
  2 in total

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