机译:非综合征性感音神经性听力障碍患者的新的和罕见的GJB2等位基因:基因型/听觉表型的相关性。
Medical Genetics Unit, Department of Mother & Child, University Hospital of Modena, Modena, Italy;
Otolaryngology Department, University Hospital of Modena, Modena, Italy;
Community Healthcare Services, Otolaryngology Department, Modena, Italy;
Medical Genetics Unit, University Hospital of Ferrara, Ferrara, Italy;
Medical Genetics Unit, Department of Mother & Child, University Hospital of Modena, Modena, Italy;
Otolaryngology Department, University Hospital of Modena, Modena, Italy;
Medical Genetics Unit, Department of Mother & Child, University Hospital of Modena, Modena, Italy,Department of Mother & Child University Hospital of Modena Via del Pozzo, 71 Modena 41124 Italy;
机译:德国335例非综合征性感音神经性听力损失患者中的GJB2突变和基因型-表型相关性:目前方法未发现其他隐性突变的证据。
机译:GJB2基因的纯合M34T突变与芬兰家庭中的常染色体隐性非综合征性感音神经性听力障碍相关
机译:编码连接蛋白26的GJB2的DNA序列分析:来自一群听力障碍病例和可变携带率,复杂基因型和对照组等位基因种族分层的观察。
机译:基于听觉滤波器带宽的梳状滤波器的设计,用于有感音神经性听力障碍的人的双耳分叉表现
机译:有和没有感觉神经性听力损失的老年听众的舒适响度范围与行为听觉动态范围之间的关系。
机译:南印度人口常染色体隐性非综合征性感觉神经性听力损失中GJB2基因3’UTR的一个新突变
机译:常染色体显性遗传的非综合征性感觉神经性听力障碍:DFNA2-DFNA13-DFNA14-DFNA21的表型和基因型相关性