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Genetic Hearing Loss by Patrick J. Willems at Abbey's Bookshop,
Genetic Hearing Loss
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Patrick J. Willems

Genetic Hearing Loss

Patrick J. Willems

$504

Hardback

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English
CRC Press Inc
17 October 2003
Medical genetics; Audiology & otology
Alone or in combination with environmental factors, heredity is at the root of most cases of hearing impairment. Thanks in large part to positional cloning techniques,

scientists have identified nearly 100 genes and loci implicated in hearing loss since 1995 - an extraordinarily rapid rate of gene mapping success. This text branches into syndromic and nonsyndromic categorical directions as a comprehensive report on this accumulated wealth of genetic discoveries.
Edited by:  
Imprint:   CRC Press Inc
Country of Publication:   United States
Dimensions:   Height: 229mm,  Width: 152mm,  Spine: 29mm
Weight:   793g
ISBN:   9780824743093
ISBN 10:   0824743091
Pages:   502
Publication Date:  
Audience:   Professional and scholarly ,  Professional and scholarly ,  Professional & Vocational ,  Undergraduate ,  Further / Higher Education
Format:   Hardback
Publisher's Status:   Active
Hearing and hearing loss: normal development of the ear in the human and mouse, audiometric tests and diagnostic workup, classification and epidemiology of hearing loss, Syndromic hearing loss: Usher syndrome, pendred syndrome, Waardenburg syndrome, Nielsensyndrome, HDR syndrome, branchio-oto-renal syndrome, Treacher Collins syndrome, MYH9, mitochondrial hearingloss, Genes responsible for nonsyndromic hearing loss: gene localization and isolation in nonsyndromic hearing loss, connexins, myosin VI, K+ channel gene KCNQ4, COL11A2, POU-Domain transcription factors, a-Tectorin P. EYA4 DFNA 5 COCH Diaphanous, Claudin 14 CDH23 TMPRSS33, otosclerosis. Miscellaneous factors: mechanisms that regulate hair cell differentiation and regeneration, genetic testing - possibilitiesand attitudes.

Patrick J. Willems

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