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All India Institute of Speech and Hearing, Mysuru
(An Autonomous institute Under Ministry of Health and Family Welfare, Government of India.)

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Genetic hearing loss / edited by Patrick J. Willems.

Contributor(s): Material type: TextPublication details: New York : Marcel Dekker, c2004.Description: xiv, 483 p. : ill. ; 24 cmISBN:
  • 0824743091 (alk. paper)
Subject(s): DDC classification:
  • 617.804 2 WIL 22
LOC classification:
  • RF292 .G455 2004
NLM classification:
  • WV 270
Online resources:
Contents:
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.
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Cover image Item type Current library Home library Collection Shelving location Call number Materials specified Vol info URL Copy number Status Notes Date due Barcode Item holds Item hold queue priority Course reserves
Reference text books All India Institute of Speech and Hearing R-56/3 617.804 2 WIL (Browse shelf) Available 13430
Stack text books All India Institute of Speech and Hearing 88/3 617.804 2 WIL (Browse shelf) Available 15995
Stack text books All India Institute of Speech and Hearing 88/3 617.804 2 WIL (Browse shelf) Available 17950
Stack text books All India Institute of Speech and Hearing 88/3 617.804 2 WIL (Browse shelf) Available 17951
Stack text books All India Institute of Speech and Hearing 88/3 617.804 2 WIL (Browse shelf) Available 17952
Stack text books All India Institute of Speech and Hearing 88/3 617.804 2 WIL (Browse shelf) Available 17953
Stack text books All India Institute of Speech and Hearing 88/3 617.804 2 WIL (Browse shelf) Available 17954
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Includes bibliographical references and index.

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.

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