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Keyword [SLC26A4 gene]
Result: 1 - 20 | Page: 1 of 2
1. Establishment And Application Of Denaturing High Performance Liquid Chromatography Technique Screening SLC26A4 Gene In Chinese Severe-Profound Hearing Impairment Population
2. Molecular Genetic Analysis Of Chinese Hearing Loss Population
3. HRCT Analysis Of Inner Ear Malformation And Deafness Gene Mutations In Chinese Pedigrees With SNHL
4. Study On Inner Ear Malformation For Its Classification And Relationship With SLC26A4 And GJB2 In Patient With Sensorineural Hearing Loss
5. Molecular Epidemiology Investigation Of Enlarged Vestibular Aqueduct Associated With SLC26A4 Gene
6. Genetic Counseling And Prenatal Diagnosis For Hearing Loss Based On Genetic Testing
7. Study On The Hot Spot Mutation Of SLC26A4 Gene And LVAS In Sensorineural Hearing Loss With Unknown Reason
8. The Enforcement And Discussion Of Strategy Of Newborn Deafness Pathogenic Screening In Shenyang, Liaoning Province Of China
9. The Molecular Epidemiology Discussion Of Newborn Deafness Pathogenic Screening
10. Investigation Of SLC26A4 Gene In Patients Associated With Sensorineural Hearing Loss In Northwest China
11. Investigation Of SLC26A4 Mutations Associated With Large Vestibular Aqueduct Syndrome And Mondini Dysplasia
12. Molecular Epidemiology Analysis Of Deaf-mute Patients In The Co-relationship Between SLC26A4 Gene And Enlargement Of Vestibular Aqueduct Among Deaf-mute Patierntes In Yunnan Province
13. Comparative Studies Of DNA Microarray And Sequencing In Genetic Diagnosis On The Patients With Enlarged Vestibular Aqueduct Syndrome
14. Large Vestibular Aqueduct Syndrome Slc26a4 Gene Mutations In Clinical Studies
15. Clinical Diagnosis Of Targe Vestibular Aqueduct Syndrome And Cochlear Intervention
16. The Analyze Of Deafness Susceptibility Gene Mutation Children Effect After Cochlear Implants
17. Molecular Etiological Study Of Cochlear Implant Patients And Analysis Of Cochlear Malformation Distribution In Cochlear Implant Patients
18. Relationship Between Deafness Mutation Of SLC26A4 Gene In The Large Vestibular Aqueduct Syndrome And High Resolution Computed Tomography Phenotype Of Temporal Bone In QingHai Area
19. Mutation Analysis Of Hereditary Deafness Family Deafness Genes And Phenotypic Prediction Of Related NsSNPs
20. Identification And Analysis A New Mutation Of The SLC26A4 Gene In A Family Of Large Vestibular Aqueduct Syndrome
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