Zhang, Hua <br/><br/>
A New Mutation Identified by Whole Exome Sequencing in a Cornelia de Lange Syndrome Newborn.  [electronic resource] 

 -  Chinese medical journal  10 2018 
 - 2384-2385 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>2542-5641 
<br/><br/><label>Standard No.: </label>10.4103/0366-6999.241793  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>De Lange Syndrome--genetics<br/>Female<br/>Humans<br/>Infant, Newborn<br/>Mutation--genetics<br/>Pedigree<br/>Exome Sequencing--methods