Schiff, E R <br/><br/>
Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease.  [electronic resource] 

 -  Human genetics  Sep 2018 
 - 723-734 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1432-1203 
<br/><br/><label>Standard No.: </label>10.1007/s00439-018-1927-7  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Case-Control Studies<br/>Female<br/>Genetic Linkage<br/>Genetic Predisposition to Disease<br/>Genetic Variation<br/>Humans<br/>Inflammatory Bowel Diseases--genetics<br/>Jews--genetics<br/>Male<br/>Nod2 Signaling Adaptor Protein--genetics<br/>Open Reading Frames<br/>Pedigree<br/>Sequence Analysis, DNA--methods