Rezultati pretrage - Senjie Du

A case report of peroneal muscle atrophy type 2A2 with central nervous system involvement as initial presentation od Xin Xu, Fen Lu, Senjie Du, Li Zhang

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Novel CLCN4 variant associated with syndromic X-linked intellectual disability in a Chinese girl: a case report od Xin Xu, Fen Lu, Li Zhang, Hongying Li, Senjie Du, Jian Tang

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Case report: Novel compound heterozygous missense mutations in the DDHD2 gene in a Chinese patient associated with spastic paraplegia type 54 od Xin Xu, Fen Lu, Senjie Du, Xiaoke Zhao, Hongying Li, Li Zhang, Jian Tang

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A de novo 10q11.23q22.1 deletion detected by whole genome mate-pair sequencing: a case report od Dalin Fu, Weisheng Lin, Fen Lu, Senjie Du, Min Zhu, Xiaoke Zhao, Jian Tang, Chuan Chen, Xiaoli Chui, Shanmei Tang, Kai Wang, Chuanchun Yang, Bei Han

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