Drost, Mark <br/><br/>
Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Jun 2013 
 - 9403-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1091-6490 
<br/><br/><label>Standard No.: </label>10.1073/pnas.1220537110  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution--genetics<br/>Base Sequence<br/>Colorectal Neoplasms, Hereditary Nonpolyposis--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Genetic Testing<br/>Genetic Variation<br/>Humans<br/>Microsatellite Repeats--genetics<br/>Models, Molecular<br/>Molecular Sequence Data<br/>MutS Homolog 2 Protein--chemistry<br/>Mutagenesis<br/>Mutation--genetics<br/>Reverse Genetics--methods<br/>Sequence Analysis, DNA<br/>Thioguanine<br/>Virulence--genetics