000 01228 a2200373 4500
005 20250517093838.0
264 0 _c20170112
008 201701s 0 0 eng d
022 _a1573-4927
024 7 _a10.1007/s10528-016-9735-z
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDemir, Emre
245 0 0 _aGenome-Wide Association Study of Copy Number Variations in Patients with Familial Neurocardiogenic Syncope.
_h[electronic resource]
260 _bBiochemical genetics
_cAug 2016
300 _a487-494 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aDNA Copy Number Variations
650 0 4 _aFemale
650 0 4 _aGenome-Wide Association Study
_xmethods
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aOligonucleotide Array Sequence Analysis
650 0 4 _aSyncope, Vasovagal
_xgenetics
650 0 4 _aYoung Adult
700 1 _aHasdemir, Can
700 1 _aAk, Handan
700 1 _aAtay, Sevcan
700 1 _aAydin, Hikmet Hakan
773 0 _tBiochemical genetics
_gvol. 54
_gno. 4
_gp. 487-494
856 4 0 _uhttps://doi.org/10.1007/s10528-016-9735-z
_zAvailable from publisher's website
999 _c25998085
_d25998085