Search Results - Chunhui Wan

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    Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review by Li Tan, Bo Bi, Peiwei Zhao, Xiaonan Cai, Chunhui Wan, Jianbo Shao, Xuelian He

    Published 2017
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