Demir, Emre <br/><br/>
Genome-Wide Association Study of Copy Number Variations in Patients with Familial Neurocardiogenic Syncope.  [electronic resource] 

 -  Biochemical genetics  Aug 2016 
 - 487-494 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1573-4927 
<br/><br/><label>Standard No.: </label>10.1007/s10528-016-9735-z  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>DNA Copy Number Variations<br/>Female<br/>Genome-Wide Association Study--methods<br/>Genotype<br/>Humans<br/>Male<br/>Oligonucleotide Array Sequence Analysis<br/>Syncope, Vasovagal--genetics<br/>Young Adult