Meyer, Robert <br/><br/>
Targeted Next Generation Sequencing Approach in Patients Referred for Silver-Russell Syndrome Testing Increases the Mutation Detection Rate and Provides Decisive Information for Clinical Management.  [electronic resource] 

 -  The Journal of pediatrics  08 2017 
 - 206-212.e1 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1097-6833 
<br/><br/><label>Standard No.: </label>10.1016/j.jpeds.2017.04.018  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child, Preschool<br/>Female<br/>High-Throughput Nucleotide Sequencing--methods<br/>Humans<br/>Infant<br/>Male<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Silver-Russell Syndrome--diagnosis