Stavropoulou, Chryssa <br/><br/>
5'RARA submicroscopic deletion from new variant translocation involving chromosomes 15, 17, and 18, in a case of acute promyelocytic leukemia.  [electronic resource] 

 -  Cancer genetics and cytogenetics  Apr 2008 
 - 50-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0165-4608 
<br/><br/><label>Standard No.: </label>10.1016/j.cancergencyto.2007.12.011  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosomes, Human, Pair 15<br/>Chromosomes, Human, Pair 17<br/>Chromosomes, Human, Pair 18<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Karyotyping<br/>Leukemia, Promyelocytic, Acute--genetics<br/>Middle Aged<br/>Receptors, Retinoic Acid--genetics<br/>Retinoic Acid Receptor alpha<br/>Sequence Deletion<br/>Translocation, Genetic