Kaseniit, Kristjan Eerik <br/><br/>
Strategies to minimize false positives and interpret novel microdeletions based on maternal copy-number variants in 87,000 noninvasive prenatal screens.  [electronic resource] 

 -  BMC medical genomics  Oct 2018 
 - 90 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1755-8794 
<br/><br/><label>Standard No.: </label>10.1186/s12920-018-0410-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>DNA Copy Number Variations<br/>Female<br/>Gene Deletion<br/>Humans<br/>Maternal Serum Screening Tests<br/>Pregnancy<br/>Prenatal Diagnosis--methods<br/>Whole Genome Sequencing