Titlebook: Genetics and Auditory Disorders; Bronya J. B. Keats,Richard R. Fay,Arthur N. Popper Book 2002 Springer Science+Business Media New York 200

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書目名稱Genetics and Auditory Disorders影響因子(影響力)




書目名稱Genetics and Auditory Disorders影響因子(影響力)學(xué)科排名




書目名稱Genetics and Auditory Disorders網(wǎng)絡(luò)公開度




書目名稱Genetics and Auditory Disorders網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Genetics and Auditory Disorders被引頻次




書目名稱Genetics and Auditory Disorders被引頻次學(xué)科排名




書目名稱Genetics and Auditory Disorders年度引用




書目名稱Genetics and Auditory Disorders年度引用學(xué)科排名




書目名稱Genetics and Auditory Disorders讀者反饋




書目名稱Genetics and Auditory Disorders讀者反饋學(xué)科排名

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0947-2657 the hearing impaired. Approaches to the diagnosis and treatment of hearing impairment have developed from technological advances in genetic research. This volume covers gene expression, mutations, mapping and cloning, as well as mitochondrial and cellular genetics. Chapters are also included on the

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0947-2657 uses of mouse models, genetic epidemiology and genetic counseling specifically for hearing impairment. As a comprehensive review of the genetics of hearing, this book will interest hearing researchers, clinicians and genetic counselors.978-1-4419-3129-0978-0-387-21853-3Series ISSN 0947-2657 Series E-ISSN 2197-1897

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Autosomal and X-Linked Auditory Disorders,urther characterization of the genes for hearing loss will provide a clearer vision of the structure and function of the auditory system in health and disease. It is hoped that these discoveries will establish a conceptual basis for the rational therapy of hearing loss and deafness.

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https://doi.org/10.1007/978-3-322-98943-7l hearing impairment have resulted in mapping of 30 autosomal dominant, 28 autosomal recessive and 5 X-linked loci for nonsyndromic hearing impairment. Physical mapping and the use of a variety of cloning approaches over the same time period have led to the identification of 18 of these genes. Furth