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Human Mutation|September 10, 2013
A short-read multiplex sequencing method for reliable, cost-effective and high-throughput genotyping in large-scale studiesHongzhi Cao, Yu Wang, Wei Zhang, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|January 26, 2018
Two de novo variations identified by massively parallel sequencing in 13 Chinese families with children diagnosed with autism spectrum disorderShi-Jun Li, Shan-Shan Yu, Hong-Yu Luo, et al.Pageof 14