Showing 1 - 3 results of 3 for search 'Victor Wei Zhang', query time: 0.03s Refine Results
  1. 1
    Case report: A novel mutation in TRPS1 identified in a Chinese family with tricho-rhino-phalangeal syndrome I: A therapeutic challenge

    Case report: A novel mutation in TRPS1 identified in a Chinese family with tricho-rhino-phalangeal syndrome I: A therapeutic challenge by Qi Huang, Cheng Jiang, Jiazhong Sun, Junli Xue, Victor Wei Zhang

    Published 2022
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  2. 2
    Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness - a case report for dual diagnosis

    Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness - a case report for dual diagnosis by Yan Zhang, Yi Zhang, Victor Wei Zhang, Chunyi Zhang, Hongke Ding, Aihua Yin

    Published 2019
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  3. 3
    Case Report: Two Chinese Infants of Sengers Syndrome Caused by Mutations in AGK Gene

    Case Report: Two Chinese Infants of Sengers Syndrome Caused by Mutations in AGK Gene by Benzhen Wang, Benzhen Wang, Zhanhui Du, Guangsong Shan, Chuanzhu Yan, Victor Wei Zhang, Zipu Li

    Published 2021
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