Valencia, Ana <br/><br/>
A new reliable fluorescence in situ hybridization method for identifying multiple specific cytogenetic abnormalities in acute myeloid leukemia.  [electronic resource] 

 -  Leukemia & lymphoma  Apr 2010 
 - 680-5 p.  digital 
<br/><br/> Publication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1029-2403 
<br/><br/><label>Standard No.: </label>10.3109/10428191003682775  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Aberrations<br/>Chromosome Inversion<br/>Chromosomes, Human, Pair 15<br/>Chromosomes, Human, Pair 16<br/>Chromosomes, Human, Pair 7<br/>DNA Mutational Analysis--methods<br/>Female<br/>Histone-Lysine N-Methyltransferase<br/>Humans<br/>In Situ Hybridization, Fluorescence--methods<br/>Leukemia, Myeloid, Acute--genetics<br/>Male<br/>Models, Biological<br/>Monosomy<br/>Myeloid-Lymphoid Leukemia Protein--genetics<br/>Oncogene Proteins, Fusion--analysis<br/>Reproducibility of Results<br/>Substrate Specificity--genetics