Sun, Yan <br/><br/>
Panel-based NGS reveals disease-causing mutations in hearing loss patients using BGISEQ-500 platform.  [electronic resource] 

 -  Medicine  Mar 2019 
 - e14860 p.  digital 
<br/><br/> Publication Type: Journal Article; Observational Study 
<br/><br/><label>ISSN: </label>1536-5964 
<br/><br/><label>Standard No.: </label>10.1097/MD.0000000000014860  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child, Preschool<br/>China<br/>DNA Copy Number Variations<br/>Female<br/>Genetic Predisposition to Disease<br/>Hearing Loss--genetics<br/>High-Throughput Nucleotide Sequencing--methods<br/>Humans<br/>Male<br/>Young Adult