000 01471 a2200445 4500
005 20250514165629.0
264 0 _c20040224
008 200402s 0 0 eng d
022 _a1468-6244
024 7 _a10.1136/jmg.2003.010702
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSnoeckx, R L
245 0 0 _aA novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3.
_h[electronic resource]
260 _bJournal of medical genetics
_cJan 2004
300 _a11-3 p.
_bdigital
500 _aPublication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
650 0 4 _aAge of Onset
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Mapping
_xmethods
650 0 4 _aChromosomes, Human, Pair 6
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
_xgenetics
650 0 4 _aGenetic Linkage
_xgenetics
650 0 4 _aGenetic Markers
_xgenetics
650 0 4 _aHearing Loss, Sensorineural
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aPedigree
650 0 4 _aSyndrome
700 1 _aKremer, H
700 1 _aEnsink, R J H
700 1 _aFlothmann, K
700 1 _ade Brouwer, A
700 1 _aSmith, R J H
700 1 _aCremers, C W R J
700 1 _aVan Camp, G
773 0 _tJournal of medical genetics
_gvol. 41
_gno. 1
_gp. 11-3
856 4 0 _uhttps://doi.org/10.1136/jmg.2003.010702
_zAvailable from publisher's website
999 _c14456161
_d14456161