Seppälä, Toni T <br/><br/>
Uptake of genetic testing by the children of Lynch syndrome variant carriers across three generations.  [electronic resource] 

 -  European journal of human genetics : EJHG  11 2017 
 - 1237-1245 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2017.132  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Child<br/>Colorectal Neoplasms, Hereditary Nonpolyposis--diagnosis<br/>DNA-Binding Proteins--genetics<br/>Female<br/>Genetic Testing--statistics & numerical data<br/>Heterozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>MutL Protein Homolog 1--genetics<br/>Mutation<br/>Pedigree