机译:深度测序揭示了50种用于隐性认知障碍的新基因
Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, 19857 Tehran, Iran Karimineiad-Najmabadi Pathology & Genetics Centre, 14667 Tehran, Iran;
Department Human Molecular Genetics, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany;
Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, 19857 Tehran, Iran Department Human Molecular Genetics, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany;
Department of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany;
Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, 19857 Tehran, Iran;
机译:丙型肝炎病毒的深度测序揭示了认知障碍患者脑脊液中的基因区隔
机译:有针对性的下一代测序揭示了
机译:下一代测序揭示了TMC1基因的新型病理突变,导致伊朗的常染色体隐性非综合征听力损失
机译:杂交瘤中的暗物质:深度测序揭示了杂交瘤细胞系中多种抗体基因的广泛表达
机译:确定普通豆中bc-1和bc-2隐性基因赋予的对豆普通花叶病毒(BCMV)的隐性抗性机理,以及一株新的BCMV菌株的生物学和分子表征
机译:丙型肝炎病毒的深度测序揭示了认知障碍患者脑脊液中的基因区隔
机译:下一个Exome测序显示出罕见的隐性疾病中的突变