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Li JR, Huang Z, Lu Y, Ji QY, Jiang MY, Yang F. Novel mutation in the ASXL3 gene in a Chinese boy with microcephaly and speech impairment: A case report. World J Clin Cases 2020; 8(24): 6465-6472 [PMID: 33392332 DOI: 10.12998/wjcc.v8.i24.6465]
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