机译:DCC的突变会导致先天性镜像运动
Cenler of Excellence in Neuromics, Universite de Montreal, Montreal, QC H2L 2W5, Canada;
Cenler of Excellence in Neuromics, Universite de Montreal, Montreal, QC H2L 2W5, Canada;
Molecular Biology of Neural Development, Institute de Recherches Cliniques de Montreal, Montreal QC H2W 1R7, Canada;
Cenler of Excellence in Neuromics, Universite de Montreal, Montreal, QC H2L 2W5, Canada Montreal Heart Institute, Montreal, QC H1T 1C8, Canada;
Cenler of Excellence in Neuromics, Universite de Montreal, Montreal, QC H2L 2W5, Canada;
Molecular Biology of Neural Development, Institute de Recherches Cliniques de Montreal, Montreal QC H2W 1R7, Canada;
Cenler of Excellence in Neuromics, Universite de Montreal, Montreal, QC H2L 2W5, Canada;
Montreal Heart Institute, Montreal, QC H1T 1C8, Canada;
Cenler of Excellence in Neuromics, Universite de Montreal, Montreal, QC H2L 2W5, Canada;
Cenler of Excellence in Neuromics, Universite de Montreal, Montreal, QC H2L 2W5, Canada;
Cenler of Excellence in Neuromics, Universite de Montreal, Montreal, QC H2L 2W5, Canada;
Department of Neurology, Jundishapour University of Medical Sciences, Ahwaz, Iran;
Cenler of Excellence in Neuromics, Universite de Montreal, Montreal, QC H2L 2W5, Canada;
Psychology, Universite de Montreal, Montreal, QC H2V 2S9, Canada;
Molecular Biology of Neural Development, Institute de Recherches Cliniques de Montreal, Montreal QC H2W 1R7, Canada;
Cenler of Excellence in Neuromics, Universite de Montreal, Montreal, QC H2L 2W5, Canada;
机译:调用症状和先天性镜子运动:与DCC DCC突变相关的结果
机译:先天性镜像:与DCC和RAD51突变相关的表型
机译:先天性镜像运动:与DCC和RAD51突变相关的表型
机译:鉴定DPAGT1作为突变引起先天性染发素综合征的新基因
机译:常染色体显性先天性白内障的基因组研究和突变功能分析。
机译:DCC突变更新:先天性镜像运动call体的孤立发育不全和发育性裂脑综合征
机译:先天性镜像运动:RAD51和DCC的突变分析26例