TY  - BOOK
AU  - Willems,Patrick J.
TI  - Genetic hearing loss
SN  - 0824743091 (alk. paper)
AV  - RF292 .G455 2004
U1  - 617.804 2 WIL 22
PY  - 2004///
CY  - New York
PB  - Marcel Dekker
KW  - Deafness
KW  - Genetic aspects
KW  - Hearing Loss
KW  - congenital
KW  - genetics
KW  - Ear
KW  - abnormalities
KW  - Molecular Biology
N1  - 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
UR  - http://www.loc.gov/catdir/enhancements/fy0647/2003062467-d.html
ER  -