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Keyword [GJB3]
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1. Collecting, Characterizing Of The Genetic Resource And Molecular Mapping Of The Relevant Genes For Hereditary Hearing Impairment
2. Study On Molecular Epidemiology And Pathogenesis Of Severe To Profound Hearing Loss In China
3. Clinical Evaluations And Mutational Analysis For Late-onset Progressive Hearing Loss
4. Mutation Screening Of The KCNQ4 And GJB3 Gene In High Frequencies Hearing Loss Population
5. The Mutation Analysis Of GJB3and GJB4Gene In A Family With Erythrakeratodermia Variabilis
6. Synchronous Detection And Follow-up On Screening Of Newborn Hearing And Deafness Gene
7. Epidemiology Investigation Of Syndrome Type Deafness Mutation Gene From Hebei Xingtai Area
8. A Analysis Of Deafness Susceptible Gene Mutation Screening For Newborns In NICU
9. Analysis Of Deafness Gene Screening In Nonsyndromic Hearing Impairment Patients In Cangzhou Of Hebei Province
10. The Genetic Analysis Based On High-throughput Sequencing In A Non-syndromic Hearing Loss Family
11. Molecular Etiological Study Of Cochlear Implant Patients And Analysis Of Cochlear Malformation Distribution In Cochlear Implant Patients
12. Analysis Of Deafness Genes Mutation In Shijiazhuang And Surrounding Areas And Identification Of A Novel Mutation Of NOG In Family With Syndrome Hearing Impairment
13. Detection Of Gene Mutations In Two Families With Epidermolytic PalmoPlantar Keratoderma And One Family With Erythrokeratodermia Variabilis
14. Comparison And Analysis Of Common Mutations In Uighur And Han Patients With Non-syndromic Deafness In Xinjiang
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