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Keyword [deafness gene]
Result: 1 - 20 | Page: 1 of 4
1. The Mutations Of Heredity Deafness Gene GJB2, PDS And Mitochondrial DNA 1555A＞G And The Development Of A New Technique Detecting The Mutations
2. Screening For Deafness Gene In Cochlear Implant Recipients
3. HRCT Analysis Of Inner Ear Malformation And Deafness Gene Mutations In Chinese Pedigrees With SNHL
4. Analysis On Mutation Of The Deafness Gene GJB2 And Clinical Application
5. The Study Of The Deafness Gene GJB2 Mutation In A Hereditary Nonsyndromic Deaf Families
6. Deafness Gene Chip For 153 Cases Of Hearing Impairment Patients Testing
7. The Research For Universal Newborn Hearing With Deafness Gene Screening Of Gansu Province
8. The Establishment For Detecting GJB2 And MtDNA A1555G And The Relation Between Genotype And Phenotype
9. The Epidemiologic Study On Newborn Hearing Combined With Deafness Gene Genotyping In Gansu Province
10. Deafness Gene Analysis Of129Patients With Non-syndromic Deafness In Taiyuan
11. Analysis Of Common Deafness Genes Mutations In Children With Profound Hearing Impairment And In Patients With Idiopathic Sudden Hearing Loss
12. Study Of Screening The Deafness Gene Of Yangzhou Children Who Are Moderate To Severe Hearing-impaired,Then Make Genetic Counseling To The Deafness Couples
13. Common Deafness Gene Characteristics Research Of Patients With Nonsyndromic Hearing Loss In Tibetan, Tu Nationality And Mongolian In The Northwest Of China
14. Analyze The Situation Of Newborn Hearing And Deafness Gene Screening In Tianjin
15. Screening Of Hot-spot Deafness Gene Mutations Among Adolescents With Hearing Loss In Yong Chuan
16. Epidemiological Investigation Of GJB2Gene Hot-spot Mutation In Deafness Disabled Populations In Beijing And Yangzhou Of China
17. Common Deafness Gene Characteristics Analysis Using SNPpscan Method Among Non-syndrome Type Deafness Patients From The Major Minority Nationalities In Xinjiang
18. Synchronous Detection And Follow-up On Screening Of Newborn Hearing And Deafness Gene
19. The Genetic Testing Of Three Waardenburg Syndrome Type Ⅱ Families
20. A Comparative Study Of Common Deafness Gene In Deaf People From Sole Minority Nationalities And The Newborn With High Risk In Gansu Province By SNPscan And Sanger Sequence
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