Search Results - Yongjia Yang

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    Case report: two novel VPS13B mutations in a Chinese family with Cohen syndrome and hyperlinear palms by Sha Zhao, Zhenqing Luo, Zhenghui Xiao, Liping Li, Rui Zhao, Yongjia Yang, Yan Zhong

    Published 2019
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    Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation by Xiulan Lu, Xiulan Lu, Weijian Chen, Weijian Chen, Liping Li, Xinyuan Zhu, Caizhi Huang, Saijun Liu, Yongjia Yang, Yaowang Zhao, Yaowang Zhao

    Published 2019
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