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Keyword [Nonsyndromic Deafness]
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1. Molecular Mechanism And Functional Characterization Associate With Maternally Inherited Aminoglycoside-induced And Nonsyndromic Deafness
2. Molecular Pathogenesis Study For An Extensive Nonsyndomic Deafness Family Associated With A1555G Mutation
3. The Study Of The Deafness Gene GJB2 Mutation In A Hereditary Nonsyndromic Deaf Families
4. The Study On The Molecular Pathogenic Mechanism Of DDOD Syndrome And Molecular Etiology Analysis Of Nonsyndromic Hearing Impairment In Southwest Of China
5. Genetic Screening Of Mutation Hot-spots For Subjects With Nonsyndromic Hearing Loss And A Novel MYO7A Gene Mutation Analysis In A Deafness Family
6. Genetic Analysis And Initial Exploration Of The Pathogenic Gene In An Autosomal Dominant Nonsyndromic Deafness Kindred
7. Molecular Mechanisms Of Deafness Induced By Mitochondrial TRNAPhe593T>C Mutations Associated With Maternally Inherited Nonsyndromic Deafness
8. Study And Application Of New Diagnostic Techniques On Genetic Deafness Genes And Molecular Genetic Study On A Family With Nonsyndromic Deafness
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