Simulation study of a fast speed trench Schottky rectifier with an isolated gate von Xu, Xianguo, Liu, Minqiang, Zeng, Chao, Chen, Wensuo

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Identification of anti-c, E alloantibodies with autoantibodies mimicking anti-c, E alloantibodies von Feng, Kangle, Huang, Xinyu, Xu, Xianguo, Shi, Xiaodi

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Six splice site variations, three of them novel, in the ABO gene occurring in nine individuals with ABO subtypes von Hong, Xiaozhen, Ying, Yanling, Zhang, Jingjing, Chen, Shu, Xu, Xianguo, He, Ji, Zhu, Faming

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The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals von Ying, Yanling, Zhang, Jingjing, Hong, Xiaozhen, Xu, Xianguo, He, Ji, Zhu, Faming

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A case of McLeod syndrome caused by a nonsense variation c.942G>A in the XK gene: A case report von Ying, Yanling, Yu, Shifang, Zhang, Jingjing, He, Ji, Xu, Xianguo, Hong, Xiaozhen, Zhu, Faming

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A study on the influence of dose rate on total ionizing dose effect of anti-fuse field programmable gate array—The irradiation damage is attenuated at low dose rate von Liu, Minqiang, Xu, Xianguo, Zeng, Chao, Xiong, Cen

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A new allele with 303 base pairs insertion in B3GALT1 gene identified in an individual with P 1 k phenotype von Hong, Xiaozhen, Huang, Xinyu, Ma, Kairong, Xu, Xianguo, Zhu, Faming

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A new allele with 303 base pairs insertion in B3GALT1 gene identified in an individual with P1k phenotype von Hong, Xiaozhen, Huang, Xinyu, Ma, Kairong, Xu, Xianguo, Zhu, Faming

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Preparation of subcooled liquid argon and test of its cooling ability von Li, Mingsheng, Sun, Yifei, Xu, Xianguo, Zhang, Shaozhi

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A novel B allele with c.736T>C, c.738C>A, and c.930A>G variations identified in a Chinese individual with Bw phenotype von Zhang, Bing, Hong, Xiaozhen, Xu, Xianguo, Zhu, Faming

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A novel B allele with c. 736T >C, c. 738C >A, and c. 930A >G variations identified in a Chinese individual with Bw phenotype von Zhang, Bing, Hong, Xiaozhen, Xu, Xianguo, Zhu, Faming

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Molecular basis of D variants in Chinese persons von Yan, Lixing, Wu, Junjie, Zhu, Faming, Hong, Xiaozhen, Xu, Xianguo

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The novel HLA‐DRB112:01:10 allele was identified by next‐generation sequencing von Chen, Nanying, Zhang, Wei, Xu, Xianguo, He, Ji, Zhu, Faming

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The novel HLA‐DRB1 12:01:10 allele was identified by next‐generation sequencing von Chen, Nanying, Zhang, Wei, Xu, Xianguo, He, Ji, Zhu, Faming

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Effect of Characterization Temperature on the Radiation Induced Degradation of Optocouplers von Xiong, Cen, Li, Heyi, Duan, Binghuang, Xu, Xianguo, Zhao, Hongchao, Chen, Quanyou, Zeng, Chao

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A Novel c.459_460insC Variation in the XK Gene Associated with McLeod Syndrome von Zhang, Bing, Yu, Shifang, Hong, Xiaozhen, Xu, Xianguo, Zhu, Faming

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A Study on X-ray Shielding Efficiency of New 3D Alloy von Liu, Minqiang, Zhu, Xiaofeng, Zeng, Chao, Xu, Xianguo

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Identification of a novel B allele with c.10‐14dupGTGTT and c.17G>A variants in a Chinese individual with a weak B phenotype von Hong, Xiaozhen, Ying, Yanling, Zhang, Jingjing, Xu, Xianguo, He, Ji, Zhu, Faming

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Identification of a novel B allele with c. 10‐14dupGTGTT and c. 17G > A variants in a Chinese individual with a weak B phenotype von Hong, Xiaozhen, Ying, Yanling, Zhang, Jingjing, Xu, Xianguo, He, Ji, Zhu, Faming

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Genetic and mechanistic evaluation of an individual with para-Bombay phenotype associated with a compound heterozygote comprising two novel FUT1 variants von Ying, Yanling, Hong, Xiaozhen, Zhang, Jingjing, Ma, Kairong, Xu, Xianguo, Zhu, Faming

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