Showing 1 - 2 results of 2 for search 'Qiuhong Xiong', query time: 0.02s Refine Results
  1. 1
    Case Report: A Missense Mutation in Dyskeratosis Congenita 1 Leads to a Benign Form of Dyskeratosis Congenita Syndrome With the Mucocutaneous Triad

    Case Report: A Missense Mutation in Dyskeratosis Congenita 1 Leads to a Benign Form of Dyskeratosis Congenita Syndrome With the Mucocutaneous Triad by Liqing Wang, Liqing Wang, Jianwei Li, Qiuhong Xiong, Qiuhong Xiong, Yong-An Zhou, Ping Li, Ping Li, Changxin Wu, Changxin Wu

    Published 2022
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  2. 2
    Identification of Two Novel Compound Heterozygous EIF2AK3 Mutations Underlying Wolcott-Rallison Syndrome in a Chinese Family

    Identification of Two Novel Compound Heterozygous EIF2AK3 Mutations Underlying Wolcott-Rallison Syndrome in a Chinese Family by Na Zhao, Yanling Yang, Ping Li, Qiuhong Xiong, Han Xiao, Changxin Wu

    Published 2021
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