Popovici, C <br/><br/>
The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1.  [electronic resource] 

 -  Blood  Feb 1999 
 - 1381-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Amino Acid Sequence<br/>Base Sequence<br/>Chromosomes, Human, Pair 6<br/>Chromosomes, Human, Pair 8<br/>Cloning, Molecular<br/>Genome, Human<br/>Hematopoietic Stem Cells--pathology<br/>Humans<br/>Leucine--genetics<br/>Male<br/>Molecular Sequence Data<br/>Myeloproliferative Disorders--genetics<br/>Oncogene Proteins--genetics<br/>Proto-Oncogene Proteins<br/>Receptors, Fibroblast Growth Factor--genetics<br/>Translocation, Genetic