机译:使用大规模平行测序对遗传性听力损失进行全面的基因检测
Department of Otolaryngology, Head and Neck Surgery, University of Iowa, Iowa City, IA 52242,Department of Molecular Physiology and Biophysics, University of Iowa Carver College of Medicine, Iowa City, IA 52242;
Department of Biomedical Engineering, University of Iowa, Iowa City, IA 52242,Center for Bioinformatics and Computational Biology, University of Iowa, Iowa City, IA 52242;
Department of Otolaryngology, Head and Neck Surgery, University of Iowa, Iowa City, IA 52242;
Department of Biomedical Engineering, University of Iowa, Iowa City, IA 52242,Center for Bioinformatics and Computational Biology, University of Iowa, Iowa City, IA 52242;
Department of Otolaryngology, Head and Neck Surgery, University of Iowa, Iowa City, IA 52242;
Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX 77030;
Department of Biomedical Engineering, University of Iowa, Iowa City, IA 52242,Center for Bioinformatics and Computational Biology, University of Iowa, Iowa City, IA 52242,Department of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, IA 52242;
Department of Otolaryngology, Head and Neck Surgery, University of Iowa, Iowa City, IA 52242,Department of Molecular Physiology and Biophysics, University of Iowa Carver College of Medicine, Iowa City, IA 52242,Interdepartmental PhD Program in Genetics, University of Iowa, Iowa City, IA 52242;
deafness; genomics; usher syndrome; diagnostics; next-generation sequencing;
机译:针对性散发性听力损失的基因测试使用靶向大规模平行测序鉴定出10种新突变
机译:通过靶向基因组捕获和大规模平行测序揭示了遗传性听力损失的新型肌球蛋白突变
机译:靶向基因组捕获和大规模平行测序,以鉴定导致中国遗传性听力损失的新变异
机译:ATP2B2基因的缺陷导致遗传性听力和小鼠和人类的失利:正常和突变PMCA2泵功能的生物物理研究
机译:单核苷酸多态性和短串联重复标记的全面大规模平行测序专家组的开发用于人类鉴定
机译:使用大规模平行测序对遗传性听力损失进行全面的基因检测
机译:使用大规模平行测序对遗传性听力损失进行全面的基因检测