000			01995cam a22003614a 4500
999			_c4138 _d4138
001			13322878
003			OSt
005			20191018153151.0
008			030825s2004 nyua b 001 0 eng
010			_a 2003062467
020			_a0824743091 (alk. paper)
035			_a(DNLM)101189365
040			_aDNLM/DLC _cDLC _dDLC
042			_apcc
050	0	0	_aRF292 _b.G455 2004
060	1	0	_aWV 270 _bG32683 2004
082	0	0	_a617.804 2 WIL _222
245	0	0	_aGenetic hearing loss / _cedited by Patrick J. Willems.
260			_aNew York : _bMarcel Dekker, _cc2004.
300			_axiv, 483 p. : _bill. ; _c24 cm.
504			_aIncludes bibliographical references and index.
505			_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.
650		0	_aDeafness _xGenetic aspects.
650	1	2	_aHearing Loss _xcongenital.
650	1	2	_aHearing Loss _xgenetics.
650	2	2	_aEar _xabnormalities.
650	2	2	_aMolecular Biology.
700	1		_aWillems, Patrick J., _d1956-
856	4	2	_3Publisher description _uhttp://www.loc.gov/catdir/enhancements/fy0647/2003062467-d.html
906			_a7 _bcbc _corignew _d1 _eocip _f20 _gy-gencatlg
942			_2ddc _cSTS