01785cam a22003134a 450000100090000000300040000900500170001300800410003001000170007102000280008803500200011604000230013604200080015905000220016706000240018908200220021324500580023526000390029330000340033250400510036650507950041765000310121265000300124365000280127365000240130165000230132570000320134885600910138013322878OSt20191018153151.0030825s2004    nyua     b    001 0 eng    a  2003062467  a0824743091 (alk. paper)  a(DNLM)101189365  aDNLM/DLCcDLCdDLC  apcc00aRF292b.G455 200410aWV 270bG32683 200400a617.804 2 WIL22200aGenetic hearing loss /cedited by Patrick J. Willems.  aNew York :bMarcel Dekker,cc2004.  axiv, 483 p. :bill. ;c24 cm.  aIncludes bibliographical references and index.  aHearing 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. 0aDeafnessxGenetic aspects.12aHearing Lossxcongenital.12aHearing Lossxgenetics.22aEarxabnormalities.22aMolecular Biology.1 aWillems, Patrick J.,d1956-423Publisher descriptionuhttp://www.loc.gov/catdir/enhancements/fy0647/2003062467-d.html