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Keyword [GJB2]
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1. Mutation Screening And Whole Spectrum Mutation Map Drawing Of GJB2 Gene Among Non-syndromic Hearing Impairment Patients
2. Study On Molecular Epidemiology And Pathogenesis Of Severe To Profound Hearing Loss In China
3. The Mutations Of Heredity Deafness Gene GJB2, PDS And Mitochondrial DNA 1555A＞G And The Development Of A New Technique Detecting The Mutations
4. The Study Of Deafness Molecular Diagnosis Technology In Clinical Application
5. Clinical Practice Of Genetic Testing For Hearing Loss
6. Molecular Genetic Analysis Of Waardenburg Syndrome And Non-syndromic Hearing Loss
7. Molecular Genetic Analysis Of Chinese Hearing Loss Population
8. The Auditory Characters For Newborns & Infants And The Deaf Gene Mutations And Genotype-Phenotype Correlations In Shandong Province
9. The Studies Of Epidemiological Characteristics And Impact Factors Of The Commone Genes In Patients With Sensorineural Hearing Loss In China
10. GJB2 (Connexin 26) Gene Mutations In 140 Patients Of Hunan Province With NSHL And Intracellular Distribution Of Two Cx26 Mutants In HeLa Cells
11. Study On Inner Ear Malformation For Its Classification And Relationship With SLC26A4 And GJB2 In Patient With Sensorineural Hearing Loss
12. Study On Prevention And Intervention For Hereditary Hearing Loss Based On Genetic Testing
13. Virulence Genes Of Two Chinese Han Hereditary Deafness Pedigrees
14. An Etiological Study On Hearing Loss Of 209 Deaf Students In Jilin Province And Mutation Analysis Of GJB2 Gene In The Congenital Deafness Cases
15. Analysis On Mutation Of The Deafness Gene GJB2 And Clinical Application
16. The Study Of GJB2 Mutation In Yi Ethnic People With Hereditary Nonsyndromic Hearing Loss Of Yunnan Province
17. Genetic Counseling And Prenatal Diagnosis For Hearing Loss Based On Genetic Testing
18. Molecular Epidemiology Investigation Of Common Deafness Genes In Chinese Northwest
19. Mutations In The GJB2 Gene In Henan Patients With Prelingual Non-syndromic Hearing Impairment
20. The Study Of The Deafness Gene GJB2 Mutation In A Hereditary Nonsyndromic Deaf Families
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