Licht, J D <br/><br/>
Clinical and molecular characterization of a rare syndrome of acute promyelocytic leukemia associated with translocation (11;17).  [electronic resource] 

 -  Blood  Feb 1995 
 - 1083-94 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Amino Acid Sequence<br/>Antineoplastic Combined Chemotherapy Protocols--therapeutic use<br/>Base Sequence<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 11<br/>Chromosomes, Human, Pair 17<br/>Cloning, Molecular<br/>DNA Primers<br/>DNA-Binding Proteins--genetics<br/>Female<br/>Humans<br/>Kruppel-Like Transcription Factors<br/>Leukemia, Promyelocytic, Acute--classification<br/>Male<br/>Middle Aged<br/>Molecular Sequence Data<br/>Polymerase Chain Reaction<br/>Promyelocytic Leukemia Zinc Finger Protein<br/>RNA, Messenger--analysis<br/>Receptors, Retinoic Acid--genetics<br/>Retinoic Acid Receptor alpha<br/>Syndrome<br/>Transcription Factors--genetics<br/>Translocation, Genetic<br/>Tretinoin--therapeutic use<br/>Zinc Fingers--genetics