Genetics and Auditory Disorders: Springer Handbook of Auditory Research, cartea 14
Editat de Bronya J. B. Keats, Richard R. Fayen Limba Engleză Hardback – 17 ian 2002
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Specificații
ISBN-13: 9780387985015
ISBN-10: 0387985018
Pagini: 340
Ilustrații: XII, 324 p.
Dimensiuni: 160 x 241 x 23 mm
Greutate: 0.68 kg
Ediția:2002
Editura: Springer
Colecția Springer Handbook of Auditory Research
Seria Springer Handbook of Auditory Research
Locul publicării:New York, NY, United States
ISBN-10: 0387985018
Pagini: 340
Ilustrații: XII, 324 p.
Dimensiuni: 160 x 241 x 23 mm
Greutate: 0.68 kg
Ediția:2002
Editura: Springer
Colecția Springer Handbook of Auditory Research
Seria Springer Handbook of Auditory Research
Locul publicării:New York, NY, United States
Public țintă
ResearchCuprins
and Overview: Genetics in Auditory Science and Clinical Audiology.- Genes and Mutations in Hearing Impairment.- Mapping and Cloning of Genes for Inherited Hearing Impairment.- Genetic Epidemiology of Deafness.- Cytogenetics and Cochlear Expressed Sequence Tags (ESTs) for Identification of Genes Involved in Hearing and Deafness.- Autosomal and X-Linked Auditory Disorders.- Hearing Loss and Mitochondrial DNA Mutations: Clinical Implications and Biological Lessons.- Mice as Models for Human Hereditary Deafness.- Genetic Counseling for Deafness.
Recenzii
From the reviews:
"This handbook represents one of the more recent additions to the expanding list of contributions arising from Springer, illuminating progress in auditory research. … this is an excellent and authoritative description of the state of the art in human auditory genetics. This area is moving so fast and, hence I recommend interested readers to get it now … ." (R. C. Trembath, Human Genetics, Vol. 114 (3), 2004)
"This handbook represents one of the more recent additions to the expanding list of contributions arising from Springer, illuminating progress in auditory research. … this is an excellent and authoritative description of the state of the art in human auditory genetics. This area is moving so fast and, hence I recommend interested readers to get it now … ." (R. C. Trembath, Human Genetics, Vol. 114 (3), 2004)