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Keyword [Non-syndromic hearing loss]
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1. Study And Application Of New Diagnostic Techniques On Deafness Genes And Molecular Epidemiology Of Hot-spot Mutations Among Non-syndromic Hearing Loss Patients In China
2. Genetic Analysis Of Non-syndromic Hearing Loss And Waardenburg Syndrome
3. Molecular Mechanism Of Late-onset Nonsyndromic Hearing Loss And Age-related, Aminoglycoside-induced Hearing Loss
4. Molecular Genetic Analysis Of Waardenburg Syndrome And Non-syndromic Hearing Loss
5. GJB2 (Connexin 26) Gene Mutations In 140 Patients Of Hunan Province With NSHL And Intracellular Distribution Of Two Cx26 Mutants In HeLa Cells
6. Establishment And Application Of Preimplantation Genetic Diagnostic Technique For Hereditary Hearing Loss And Study Of Molecular Mechanism Of Inherited Deafness Pedigrees
7. Clinical Investigation Of A Huge Family With Autosomal Dominant Hereditary Non-syndromic Hearing Loss
8. Molecular Finding In Two Chinese Families With Nonsyndromic Hearing Impairment
9. Gene Localization And A Novel Mutation Identified For Non-syndromic Hearing Loss
10. Analyzing The Hereditary Features And The DNA Mutations In A Large Pedigree With Non-sensoneural Hearing Loss
11. Optimization And Application Of Genetic Diagnostic System For Hereditary Nonsyndromic Hearing Loss
12. Mutation Maps Drawing And Analysis Of Common Deafness Genes Among Non-syndromic Hearing Loss In Northwest China
13. The Relativity Study Of The Mitochondrial Gene Mutation Of Non-syndromic Hearing Loss And Kidney Deficiency With Blood Stasis Type Of Uigur And Han
14. Molecular Genetic Characterization Of Two Chinese Pedigrees With Aminoglycoside-induced And Non-syndromic Hearing Loss
15. Sequence Analysis Of The Complete Mitochondrial Genome And TRMU Gene Of Two Pedigrees With Hearing Impairment Associated With The 12S RRNA A827G Mutation
16. Sequence Analysis Of Mitochondrial 12S RRNA And TRNASer(UCN) Genes In Patients With Non-syndromic Hearing Loss
17. Mutational Analysis Of SLC26A5 IVS2-2A>G In Chinese Han Patients With Non-syndromic Hearing Loss
18. The Relativity Study Of The Mitochondrial Gene Mutation Of Non-syndromic Hearing Loss And Kidney Deficiency With Blood Stasis Type Of Uigur And Han
19. Sequence Analysis Of Mitochondrial 12s Rrna And Trnaser(ucn) Genes In Patients With Non-syndromic Hearing Loss
20. Mutational Analysis Of Slc26a5 Ivs2-2a>g In Chinese Han Patients With Non-syndromic Hearing Loss
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