Menéndez, M <br/><br/>
Founder effect of a pathogenic MSH2 mutation identified in Spanish families with Lynch syndrome.  [electronic resource] 

 -  Clinical genetics  Aug 2010 
 - 186-90 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2009.01346.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alternative Splicing--genetics<br/>Colorectal Neoplasms, Hereditary Nonpolyposis--genetics<br/>Exons--genetics<br/>Family<br/>Female<br/>Founder Effect<br/>Haplotypes--genetics<br/>Humans<br/>Male<br/>MutS Homolog 2 Protein--genetics<br/>Pedigree<br/>Spain