HearingImpairment相关论文
A Novel Nonsense Mutation in MYO6 Is Associated With Progressive Nonsyndromic Hearing Loss in a Chin
Objective: To characterize a Chinese DFNA22 family associated with a novel MYO6 mutation and to confirm the proposed gen......
High De Novo Rate of Dominant GJB2 Mutations in Chinese Han patients with Hearing Impairment and Pal
Objective: Dominant mutations in GJB2 may lead to various degrees of sensorineural hearing impairment and/or hyperprolif......
Hereditary nonsyndromic hearing loss (NSHL) is extremely heterogeneous.During the past decade, remarkable progress has b......
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目的探讨不同胎龄早产儿及多种高危因素与听力损失程度的关系,为临床诊断、治疗提供可靠依据。方法选取2010年1月至2012年6月入住......
目的探讨影响重度高胆红素血症新生儿听力损伤预后情况的相关因素。方法选择2008年11月至2009年10月本院新生儿科收治的重度高胆红......
目的 掌握中国听力残疾人群现状及致残原因.方法 采用统计描述和统计推理等方法对第二次全国残疾人抽样调查数据进行分析.结果 中......
Single nucleotide polymorphisms and haplotypes analysis of DFNB1 locus in Chinese sporadic hearing i
Background The DFNB1 locus, which contains the gap junction beta-2 (GJB2) and gap junction beta-6 (GJB6) genes, plays a ......
