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