000 01535 a2200433 4500
005 20250516062909.0
264 0 _c20120430
008 201204s 0 0 eng d
022 _a1552-4833
024 7 _a10.1002/ajmg.a.34302
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSchönewolf-Greulich, Bitten
245 0 0 _aTwo new cases with microdeletion of 17q23.2 suggest presence of a candidate gene for sensorineural hearing loss within this region.
_h[electronic resource]
260 _bAmerican journal of medical genetics. Part A
_cDec 2011
300 _a2964-9 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 17
650 0 4 _aComparative Genomic Hybridization
650 0 4 _aFemale
650 0 4 _aHearing Loss, Sensorineural
_xdiagnosis
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aT-Box Domain Proteins
_xgenetics
700 1 _aRonan, Anne
700 1 _aRavn, Kristine
700 1 _aBaekgaard, Peter
700 1 _aLodahl, Marianne
700 1 _aNielsen, Kate
700 1 _aRendtorff, Nanna D
700 1 _aTranebjaerg, Lisbeth
700 1 _aBrøndum-Nielsen, Karen
700 1 _aTümer, Zeynep
773 0 _tAmerican journal of medical genetics. Part A
_gvol. 155A
_gno. 12
_gp. 2964-9
856 4 0 _uhttps://doi.org/10.1002/ajmg.a.34302
_zAvailable from publisher's website
999 _c21282687
_d21282687