Search Results - Xiao-Fen Zhan

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    Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia by Hui Yang, Qian Wang, Lei Zheng, Xiang-bin Zheng, Min Lin, Xiao-Fen Zhan, Li-Ye Yang

    Published 2016
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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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