Search Results - Lanlan Mi

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    Concurrent de novo MACF1 mutation and inherited 16p13.11 microduplication in a preterm newborn with hypotonia, joint hyperlaxity and multiple congenital malformations: a case repor... by Lanlan Mi, Ruen Yao, Weiwei Guo, Jian Wang, Guoqing Zhang, Xiuxia Ye

    Published 2024
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