Genetics of Auditory Disorders:
Genetics is fundamental to hearing function, and an understanding of genetics enhances both auditory research and the clinical treatment of the hearing impaired. Approaches to the diagnosis and treatment of hearing impairment have developed from technological advances in genetic research. This volum...
Gespeichert in:
Weitere Verfasser: | , , |
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Format: | Elektronisch E-Book |
Sprache: | English |
Veröffentlicht: |
New York, NY
Springer New York
2002
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Schriftenreihe: | Springer Handbook of Auditory Research
14 |
Schlagworte: | |
Online-Zugang: | UBR01 Volltext |
Zusammenfassung: | Genetics is fundamental to hearing function, and an understanding of genetics enhances both auditory research and the clinical treatment of 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 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 |
Beschreibung: | 1 Online-Ressource (XII, 324 p) |
ISBN: | 9780387218533 |
DOI: | 10.1007/b97653 |
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Datensatz im Suchindex
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discipline | Biologie |
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spelling | Genetics of Auditory Disorders edited by Bronya J. B. Keats, Richard R. Fay, Arthur N. Popper New York, NY Springer New York 2002 1 Online-Ressource (XII, 324 p) txt rdacontent c rdamedia cr rdacarrier Springer Handbook of Auditory Research 14 Genetics is fundamental to hearing function, and an understanding of genetics enhances both auditory research and the clinical treatment of 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 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 Animal Physiology Neurosciences Human Physiology Animal physiology Human physiology Hörstörung (DE-588)4025437-9 gnd rswk-swf Angeborene Krankheit (DE-588)4331107-6 gnd rswk-swf (DE-588)4143413-4 Aufsatzsammlung gnd-content Hörstörung (DE-588)4025437-9 s Angeborene Krankheit (DE-588)4331107-6 s DE-604 Keats, Bronya J. B. edt Fay, Richard R. edt Popper, Arthur N. edt Erscheint auch als Druck-Ausgabe 9781441931290 Erscheint auch als Druck-Ausgabe 9780387985015 Erscheint auch als Druck-Ausgabe 9781475777307 https://doi.org/10.1007/b97653 Verlag URL des Erstveröffentlichers Volltext |
spellingShingle | Genetics of Auditory Disorders Animal Physiology Neurosciences Human Physiology Animal physiology Human physiology Hörstörung (DE-588)4025437-9 gnd Angeborene Krankheit (DE-588)4331107-6 gnd |
subject_GND | (DE-588)4025437-9 (DE-588)4331107-6 (DE-588)4143413-4 |
title | Genetics of Auditory Disorders |
title_auth | Genetics of Auditory Disorders |
title_exact_search | Genetics of Auditory Disorders |
title_full | Genetics of Auditory Disorders edited by Bronya J. B. Keats, Richard R. Fay, Arthur N. Popper |
title_fullStr | Genetics of Auditory Disorders edited by Bronya J. B. Keats, Richard R. Fay, Arthur N. Popper |
title_full_unstemmed | Genetics of Auditory Disorders edited by Bronya J. B. Keats, Richard R. Fay, Arthur N. Popper |
title_short | Genetics of Auditory Disorders |
title_sort | genetics of auditory disorders |
topic | Animal Physiology Neurosciences Human Physiology Animal physiology Human physiology Hörstörung (DE-588)4025437-9 gnd Angeborene Krankheit (DE-588)4331107-6 gnd |
topic_facet | Animal Physiology Neurosciences Human Physiology Animal physiology Human physiology Hörstörung Angeborene Krankheit Aufsatzsammlung |
url | https://doi.org/10.1007/b97653 |
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