Search Results - Hanbing Xie

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    A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case report by Cong Zhou, Yuanyuan Xiao, Hanbing Xie, Shanling Liu, Jing Wang

    Published 2021
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    Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected family by Jing Chen, Qinqin Xiang, Xiao Xiao, Bocheng Xu, Hanbing Xie, He Wang, Mei Yang, Shanling Liu

    Published 2022
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