000 | 01793 a2200565 4500 | ||
---|---|---|---|
005 | 20250513204231.0 | ||
264 | 0 | _c20000330 | |
008 | 200003s 0 0 eng d | ||
022 | _a0023-852X | ||
024 | 7 |
_a10.1097/00005537-200003000-00025 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aAdmiraal, R J | |
245 | 0 | 0 |
_aHearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation. _h[electronic resource] |
260 |
_bThe Laryngoscope _cMar 2000 |
||
300 |
_a457-61 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAge Factors |
650 | 0 | 4 | _aAnalysis of Variance |
650 | 0 | 4 | _aAudiometry |
650 | 0 | 4 | _aAuditory Threshold |
650 | 0 | 4 |
_aBone Conduction _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 12 _xgenetics |
650 | 0 | 4 |
_aCleft Palate _xgenetics |
650 | 0 | 4 |
_aConnective Tissue Diseases _xgenetics |
650 | 0 | 4 | _aCross-Sectional Studies |
650 | 0 | 4 | _aDisease Progression |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aGenetic Linkage _xgenetics |
650 | 0 | 4 |
_aHearing Loss, Conductive _xgenetics |
650 | 0 | 4 |
_aHearing Loss, Sensorineural _xgenetics |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aLinear Models |
650 | 0 | 4 | _aLongitudinal Studies |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 |
_aMutation _xgenetics |
650 | 0 | 4 |
_aMyopia _xgenetics |
650 | 0 | 4 |
_aOtitis Media _xgenetics |
650 | 0 | 4 |
_aPresbycusis _xgenetics |
650 | 0 | 4 | _aPrevalence |
650 | 0 | 4 |
_aProcollagen _xgenetics |
650 | 0 | 4 | _aSyndrome |
700 | 1 | _aBrunner, H G | |
700 | 1 | _aDijkstra, T L | |
700 | 1 | _aHuygen, P L | |
700 | 1 | _aCremers, C W | |
773 | 0 |
_tThe Laryngoscope _gvol. 110 _gno. 3 Pt 1 _gp. 457-61 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1097/00005537-200003000-00025 _zAvailable from publisher's website |
999 |
_c10672316 _d10672316 |