Andrew, Susan E <br/><br/>
An intronic polymorphism of the hMLH1 gene contributes toward incomplete genetic testing for HNPCC.  [electronic resource] 

 -  Genetic testing  2002 
 - 319-22 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1090-6576 
<br/><br/><label>Standard No.: </label>10.1089/10906570260471868  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing<br/>Base Sequence<br/>Carrier Proteins<br/>Colorectal Neoplasms, Hereditary Nonpolyposis--genetics<br/>DNA Primers<br/>Female<br/>Humans<br/>Introns<br/>Male<br/>Molecular Sequence Data<br/>MutL Protein Homolog 1<br/>Neoplasm Proteins--genetics<br/>Nuclear Proteins<br/>Pedigree<br/>Polymorphism, Genetic