Search Results - Jia-Xin Xu

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  1. 1
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    Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong by Jia-Xin Xu, Fen Lin, Zi-Kai Chen, Zhao-Yun Luo, Xiao-Fen Zhan, Jiao-Ren Wu, Yu-Bin Ma, Jian-Dong Li, Li-Ye Yang

    Published 2021
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  2. 2
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    UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China by 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

    Published 2021
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  3. 3
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    UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice by Zhe Yang, Fen Lin, Jia-Xin Xu, Hui Yang, Yong-Hao Wu, Zi-Kai Chen, He Xie, Bin Huang, Wei-Hao Lin, Jian-Peng Wu, Yu-Bin Ma, Jian-Dong Li, Li-Ye Yang

    Published 2022
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