Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE
利用阵列比较基因组杂交（array CGH）技术检测自闭症家族基因组中外显子拷贝数变异，发现TMLHE基因存在一个新的缺失。
期刊:Human Molecular Genetics
影响因子:3.1
doi:10.1093/hmg/ddr363.
Patricia B S Celestino-Soper ,Chad A Shaw, Stephan J Sanders, Jian Li, Michael T Murtha, A Gulhan Ercan-Sencicek, Lea Davis, Susanne Thomson, Tomasz Gambin, A Craig Chinault, Zhishuo Ou, Jennifer R German, Aleksandar Milosavljevic, James S Sutcliffe, Edwin H Cook Jr, Pawel Stankiewicz, Matthew W State, Arthur L Beaudet
