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0 积分 2025-10-17 加入
Hearing loss in patients with osteogenesis imperfecta. A clinical and audiological study of 201 patients
1个月前
已完结
Clinical application of whole exome sequencing (WES) in the genetic diagnosis of 768 Chinese patients with bilateral hearing loss
8个月前
已完结
Mechano-electrical transduction components TMC1-CIB2 undergo a Ca2+-induced conformational change linked to hearing loss
8个月前
已完结
Targeted Next-Generation Sequencing Analysis Reveals a Novel Genetic Variant in MYO6 Gene in an Indian Family with Postlingual Nonsyndromic Hearing Loss
10个月前
已完结
Genetic etiology of non-syndromic hearing loss in Europe
10个月前
已完结
Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of humanDIAPH1-related cytoskeletopathy
10个月前
已完结
A novel frameshift mutation in the DIAPH1 gene causes a Chinese family autosomal dominant nonsyndromic hearing loss
10个月前
已完结
Genetic analysis of patients with low-frequency non-syndromic hearing loss
10个月前
已完结
Identification of a novel DFNA5 mutation, IVS7-2 a > G, in a Chinese family with non-syndromic sensorineural hearing loss
10个月前
已完结
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