Search Results - Qiwei Guo

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    Recurrent c.G1636A (p.G546S) mutation of COL2A1 in a Chinese family with skeletal dysplasia and different metaphyseal changes: a case report by Jing Chen, Xiaomin Ma, Yulin Zhou, Guimei Li, Qiwei Guo

    Published 2017
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    A de novo frameshift variant of ANKRD11 (c.1366_1367dup) in a Chinese patient with KBG syndrome by Jing Chen, Zhongmin Xia, Yulin Zhou, Xiaomin Ma, Xudong Wang, Qiwei Guo

    Published 2021
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