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Keyword [SLC26A4]
Result: 1 - 20 | Page: 1 of 4
1. Study On Molecular Epidemiology And Pathogenesis Of Severe To Profound Hearing Loss In China
2. Establishment And Application Of Denaturing High Performance Liquid Chromatography Technique Screening SLC26A4 Gene In Chinese Severe-Profound Hearing Impairment Population
3. The Study Of Deafness Molecular Diagnosis Technology In Clinical Application
4. Clinical Practice Of Genetic Testing For Hearing Loss
5. Molecular Genetic Analysis Of Waardenburg Syndrome And Non-syndromic Hearing Loss
6. Mutation Detection And Functional Study Of Related Genes Of Enlarged Vestibular Aqueduct Syndrome
7. Molecular Genetic Analysis Of Chinese Hearing Loss Population
8. HRCT Analysis Of Inner Ear Malformation And Deafness Gene Mutations In Chinese Pedigrees With SNHL
9. The Auditory Characters For Newborns & Infants And The Deaf Gene Mutations And Genotype-Phenotype Correlations In Shandong Province
10. The Studies Of Epidemiological Characteristics And Impact Factors Of The Commone Genes In Patients With Sensorineural Hearing Loss In China
11. The Study Of Copy Number Variation, KCNJ10 Gene Screening And Expression In Patients With Non-syndromic Enlarged Vestibular Aqueduct
12. Study On Inner Ear Malformation For Its Classification And Relationship With SLC26A4 And GJB2 In Patient With Sensorineural Hearing Loss
13. Molecular Epidemiology Investigation Of Enlarged Vestibular Aqueduct Associated With SLC26A4 Gene
14. Genetic Counseling And Prenatal Diagnosis For Hearing Loss Based On Genetic Testing
15. Molecular Epidemiology Investigation Of Common Deafness Genes In Chinese Northwest
16. Study On The Hot Spot Mutation Of SLC26A4 Gene And LVAS In Sensorineural Hearing Loss With Unknown Reason
17. Association Studies On Susceptibility Loci (Gene) Of Two Types Of Non-syndromic Hearing Impairment
18. Clinical Epidemiology And Molecular Epidemiology Analysis Of Deaf-mutes Students In Gansu Province
19. Clinical Analysis And Genetic Detection In 4 Cases Of Large Vesticular Aquedeuct Syndrome
20. Analysis Of The Relatoin Between Gene Mutation And Clinical Phenotype For Autosomal Recessive Families
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