Smith, Alexandra G <br/><br/>
A common genetic variant in XPD associates with risk of 5q- and 7q-deleted acute myeloid leukemia.  [electronic resource] 

 -  Blood  Feb 2007 
 - 1233-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Standard No.: </label>10.1182/blood-2006-07-037853  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acute Disease<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 5<br/>Chromosomes, Human, Pair 7<br/>Genetic Predisposition to Disease<br/>Genetic Variation<br/>Glutamine<br/>Humans<br/>Leukemia, Myeloid--epidemiology<br/>Prognosis<br/>Xeroderma Pigmentosum Group D Protein--genetics