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Keyword [Hereditary hearing loss]
Result: 1 - 20 | Page: 1 of 3
1. Collecting, Characterizing Of The Genetic Resource And Molecular Mapping Of The Relevant Genes For Hereditary Hearing Impairment
2. Mapping And Cloning The Causative Genes In Chinese Pedigrees With Hereditary Hearing Loss And Molecular Epidemiology Of Connexins In Sporadic Population With Hereditary Hearing Loss
3. The Study Of Molecular Mechanism In Mitochondrial DNA Mutations Related Hearing Loss
4. Mapping And Postional Cloning The Causative Genes In Chinese Pedigrees With Non-syndromic Hereditary Hearing Impairment
5. Molecular Epidemiology And Mechanism Study Of Mitochondrial DNA A1555G Mutation In Hearing Impairment
6. Study Of Molecular Mechanism Of Autosomal Dominant Nonsyndromic Hereditary Hearing Loss And Pfeiffer Syndrome
7. Study Of Molecular Mechanism Of Non-syndromic Hereditary Hearing Loss
8. Establishment And Application Of Preimplantation Genetic Diagnostic Technique For Hereditary Hearing Loss And Study Of Molecular Mechanism Of Inherited Deafness Pedigrees
9. Study On Prevention And Intervention For Hereditary Hearing Loss Based On Genetic Testing
10. Exome Sequencing In Gene Identification In Recessive Hereditary Hearing Loss And Pheno Type-genotype Correlation
11. The Genetic Study For Auditory Neuropathy
12. Mutation Screening Of The KCNQ4 And GJB3 Gene In High Frequencies Hearing Loss Population
13. The Study Of GJB2 Mutation In Yi Ethnic People With Hereditary Nonsyndromic Hearing Loss Of Yunnan Province
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. Clinical Analysis Of A Waardenburg Syndrome Type 2 Family And Mutation Detection For MITF Gene
17. Gene Localization And A Novel Mutation Identified For Non-syndromic Hearing Loss
18. Mapping And Identified The Causative Genes In Chinese Nonsyndromic X-linked Hereditary Hearing Loss Pedigrees
19. Mutation Screening Of SOX10 Gene In One Chinese Family With Waardenburg Syndrome Type 2
20. A Relative Study On The Patients With Non-syndromic Hereditary Hearing Loss Of GJB2 Gene Mutations And Kidney Deficiency And Blood Stasis In Uyghur And Han In Xinjiang
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