Search Results - Shiyue Mei

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  1. 1
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    Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and homocystinuria by Shuang Hu, Shiyue Mei, Ning Liu, Xiangdong Kong

    Published 2018
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  2. 2
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    Status epilepticus due to fructose‐1,6‐bisphosphatase deficiency caused by FBP1 gene mutation by Shiyue Mei, Chao Ma, Yibing Cheng, Suyun Qian, Zhipeng Jin

    Published 2019
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    Clinical and genetic analysis of two patients with primary ciliary dyskinesia caused by a novel variant of DNAAF2 by Lili Dong, Lei Zhang, Xiao Li, Shiyue Mei, Yuelin Shen, Libing Fu, Shunying Zhao, Xiaolei Tang, Yu Tang

    Published 2023
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    Case Report: Clinical manifestations and treatment of two Chinese patients with FINCA syndrome carrying a novel variant of NHLRC2 by Yuemei Liu, Hongling Wang, Yu Tang, Lei Zhang, Yanyan Su, Yanqion Wang, Shasha Xu, Shiyue Mei, Chunyang Jia, Yuelin Shen, Xiaolei Tang

    Published 2024
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