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Keyword [deafness gene]
Result: 41 - 60 | Page: 3 of 4
41. A Study Of Common Deafness Genes Using The Combination SNPscan And Sanger Sequencing In Nonsyndromic Hearing Loss Patients Of Minority In Northwest China And Mutation Analysis Of 9 Uncommon Deafness Genes Using SNPscan
42. Analysis Of Genetic Screening Of Mutations In Patients With Sensorineural Hearing Loss In YanBian Area
43. Detection And Analysis Of Common Deafness Genes In The North Of Anhui Province
44. Preliminary Mapping Of A Non-syndromic Autosomal Dominant Hereditary Deafness Gene By A Next Generation Sequencing Technique
45. Neonatal Hearing Screening Combined With Deafness Gene Clinical Significance Of Screening
46. Study On Cytotoxicity Induced By Truncated Mutation Of Deafness Gene DFNA5
47. Retrospective Analysis Of 73 Cases Of Cochlear Implantation In Children
48. Analysis Of Hot-spot Gene Screening For Deafness And Its Postoperative Effect In Patients With Cochlear Implant
49. Screening Analysis Of Common Hereditary Deafness Gene Mutation In High Risk Individuals Of Changchun
50. In-depth Study Of GJB2 Gene Mutation Site Based On The Follow-up Results Of Newborn Deafness Gene Screening In Zhengzhou
51. The Study Of Deafness Gene Mutation And The Effect Of The Cochlear Implantation
52. Deafness Gene Detection And MYO15A Gene Mutation Analysis In Special Education Schools In Yunnan
53. Analysis Of 58363 Cases Of Deafness Gene Screening In Shenzhen City And Discussion On Technology Development
54. The Analysis Of Common Deafness Genes In Deaf Patients Of Mongolian And Han Nationalities In Inner Mongolia
55. Comparative Study Of Gene Chip Technology And High-Throughput Sequencing Technology In The Diagnosis Of Deafness
56. The Analysis Of The Results Of The Screening Of The Hearing-screening Combined Deafness Gene Of Children In The Northeast Of Sichuan
57. Genetic Mapping And Gene Diagnosis For Inherited Deafness Pedigrees
58. Imaging And Deafness Gene Research Of Severe To Profoud Hearing Loss Patients In Guangxi Region
59. Study On The Carrying Status Of Causative Genes For Non-syndromic Deafness Of Newborns In Inner Mongolia
60. Screening And Analysis Of Mutation In Deafness-associated Genes Among Newborns Of Ethnic Groups In Dali Area
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