Sikkema-Raddatz, Birgit <br/><br/>
Targeted next-generation sequencing can replace Sanger sequencing in clinical diagnostics.  [electronic resource] 

 -  Human mutation  Jul 2013 
 - 1035-42 p.  digital 
<br/><br/> Publication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.22332  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cardiomyopathies--diagnosis<br/>Cardiomyopathy, Dilated--diagnosis<br/>Exons<br/>High-Throughput Nucleotide Sequencing--methods<br/>Humans<br/>Mutation<br/>Reproducibility of Results<br/>Sensitivity and Specificity<br/>Sequence Analysis, DNA--methods