Sawyer, S L <br/><br/>
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care.  [electronic resource] 

 -  Clinical genetics  Mar 2016 
 - 275-84 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.12654  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Canada<br/>Child<br/>Exome<br/>Genes<br/>Genetic Diseases, Inborn--diagnosis<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Mutation<br/>Sequence Analysis, DNA