Xu, L <br/><br/>
Molecular cytogenetic characterization and clinical relevance of additional, complex and/or variant chromosome abnormalities in acute promyelocytic leukemia.  [electronic resource] 

 -  Leukemia  Sep 2001 
 - 1359-68 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0887-6924 
<br/><br/><label>Standard No.: </label>10.1038/sj.leu.2402205  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Child<br/>Chromosome Aberrations<br/>Chromosome Disorders<br/>Chromosome Painting<br/>Chromosomes, Human, Pair 15<br/>Chromosomes, Human, Pair 17<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Karyotyping<br/>Leukemia, Promyelocytic, Acute--genetics<br/>Male<br/>Middle Aged<br/>Prognosis<br/>Translocation, Genetic