Rostasy, K <br/><br/>
Modification of risk for cancer as a coincidental finding in DNA array investigation.  [electronic resource] 

 -  Clinical genetics  Mar 2013 
 - 284-7 p.  digital 
<br/><br/> Publication Type: Case Reports; 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.1399-0004.2012.01881.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Checkpoint Kinase 2<br/>Chromosome Deletion<br/>Chromosome Disorders--diagnosis<br/>Chromosomes, Human, Pair 22--genetics<br/>Female<br/>Humans<br/>Incidental Findings<br/>Magnetic Resonance Imaging<br/>Neurofibromin 2--genetics<br/>Neuroma, Acoustic--diagnosis<br/>Oligonucleotide Array Sequence Analysis--methods<br/>Protein Serine-Threonine Kinases--genetics<br/>Risk Factors