...
机译:在中国家庭中鉴定与非思想逐步听力损失相关的新型CDH23基因变异:遗传诊断指导的个性化听证康复
Shanghai Jiao Tong Univ Sch Med Peoples Hosp 9 Dept Otolaryngol Head &
Neck Surg Shanghai;
Shanghai Jiao Tong Univ Sch Med Peoples Hosp 9 Dept Otolaryngol Head &
Neck Surg Shanghai;
Shanghai Jiao Tong Univ Sch Med Peoples Hosp 9 Dept Otolaryngol Head &
Neck Surg Shanghai;
Shanghai Jiao Tong Univ Sch Med Peoples Hosp 9 Dept Otolaryngol Head &
Neck Surg Shanghai;
Shanghai Jiao Tong Univ Sch Med Peoples Hosp 9 Dept Otolaryngol Head &
Neck Surg Shanghai;
Shanghai Jiao Tong Univ Sch Med Peoples Hosp 9 Dept Otolaryngol Head &
Neck Surg Shanghai;
Shanghai Jiao Tong Univ Sch Med Peoples Hosp 9 Dept Otolaryngol Head &
Neck Surg Shanghai;
Shanghai Jiao Tong Univ Sch Med Peoples Hosp 9 Dept Otolaryngol Head &
Neck Surg Shanghai;
Shanghai Jiao Tong Univ Sch Med Peoples Hosp 9 Dept Otolaryngol Head &
Neck Surg Shanghai;
Shanghai Jiao Tong Univ Sch Med Peoples Hosp 9 Dept Otolaryngol Head &
Neck Surg Shanghai;
Non-syndromic hearing loss; Progressive hearing loss; CDH23; Genetic diagnosis; Hearing rehabilitation;
机译:在中国家庭中鉴定与非思想逐步听力损失相关的新型CDH23基因变异:遗传诊断指导的个性化听证康复
机译:GJB2基因新的致病变异的鉴定和临床意义导致近亲伊朗家庭中的常染色体隐性非综合征听力损失
机译:连接蛋白26 M34T变体的遗传分析:鉴定M34T / M34T基因型与轻度中度非综合征性感音神经性听力损失分离。
机译:AudioGene:基于计算机的非综合征性听力障碍涉及的遗传因素预测
机译:听力母亲对儿童听力损失的识别解决方案:对诊断访谈反应的探索
机译:GJB2基因中新型致病变异的鉴定和临床意义导致近亲伊朗家庭中的常染色体隐性非综合征性听力损失
机译:连接蛋白26 M34T变体的遗传分析:鉴定M34T / M34T基因型与轻度中度非综合征性感音神经性听力损失