Griffiths, M <br/><br/>
Acquired isodisomy for chromosome 13 is common in AML, and associated with FLT3-itd mutations.  [electronic resource] 

 -  Leukemia  Dec 2005 
 - 2355-8 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>0887-6924 
<br/><br/><label>Standard No.: </label>10.1038/sj.leu.2403988  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acute Disease<br/>Aged<br/>Child, Preschool<br/>Chromosomes, Human, Pair 13<br/>Female<br/>Humans<br/>Leukemia, Myeloid--genetics<br/>Male<br/>Middle Aged<br/>Mutation<br/>Tandem Repeat Sequences<br/>Uniparental Disomy<br/>fms-Like Tyrosine Kinase 3--genetics