Solassol, Jérôme <br/><br/>
Alu element insertion in the MLH1 exon 6 coding sequence as a mutation predisposing to Lynch syndrome.  [electronic resource] 

 -  Human mutation  06 2019 
 - 716-720 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.23725  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Alu Elements<br/>Colorectal Neoplasms, Hereditary Nonpolyposis--genetics<br/>Exons<br/>Female<br/>Genetic Predisposition to Disease<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Male<br/>MutL Protein Homolog 1--genetics<br/>Mutagenesis, Insertional<br/>Pedigree<br/>Phenotype<br/>Sequence Analysis, DNA--methods