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Keyword [nonsyndromic hearing loss]
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1. Molecular Mechanism Of Late-onset Nonsyndromic Hearing Loss And Age-related, Aminoglycoside-induced Hearing Loss
2. Molecular Genetic Analysis Of Chinese Hearing Loss Population
3. Cochlear Implantation And Related Basic And Clinical Studies In The Children With Profound Sensorineural Hearing Loss And Inner Ear Malformation
4. The Study Of GJB2 Mutation In Yi Ethnic People With Hereditary Nonsyndromic Hearing Loss Of Yunnan Province
5. Study On The Mitochondrial DNA Mutation And The Phenotype Diversity Of Nonsyndromic Hearing Loss
6. Optimization And Application Of Genetic Diagnostic System For Hereditary Nonsyndromic Hearing Loss
7. Molecular Pathogenesis On The Mitochondrial TRNAHis12201T>C Mutation Associated Maternally Transmitted With Nonsyndromic Hearing Loss
8. Genetic Screening Of Mutation Hot-spots For Subjects With Nonsyndromic Hearing Loss And A Novel MYO7A Gene Mutation Analysis In A Deafness Family
9. Common Deafness Gene Characteristics Research Of Patients With Nonsyndromic Hearing Loss In Tibetan, Tu Nationality And Mongolian In The Northwest Of China
10. Hot Mutations Detection Of The Deafness By Using Multiple Single Nucleotide Primer Extension
11. Genetic Analysis Of A Family With Autosomal Dominant Nonsyndromic Hearing Loss
12. Molecular Mechanisms Of Deafness Induced By Mitochondrial TRNAPhe593T>C Mutations Associated With Maternally Inherited Nonsyndromic Deafness
13. Analysis Of GJB2,SLC26A4 And Mitochondrial DNA Mutation In Hani Ethnic Patients With Nonsyndromic Hearing Loss From Yunnan
14. Detection And Clinical Phenotype Analysis Of Five Deafness Related Mitochondrial Candidate Genes In Patients With Nonsyndromic Hearing Loss
15. A Study Of Common Deafness Genes Using The Combination SNPscan And Sanger Sequencing In Nonsyndromic Hearing Loss Patients Of Minority In Northwest China And Mutation Analysis Of 9 Uncommon Deafness Genes Using SNPscan
16. The Study On Whole Exome Sequencing Of Deafness Gene In Pedigrees Of Non-syndromic Hearing Loss In Guangxi Region
17. Pathogenesis Of Digenic Variants In Nonsyndromic Hearing Loss
18. Preliminary Study On The Pathogenicity And Pathogenic Mechanism Of A Variant In 5’UTR Of Novel Deafness Gene EPHA10
19. Application Study Of Genetic Diagnosis In Nonsyndromic Hearing Loss By Suspension Array Technology
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