Maljaei, S H <br/><br/>
Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic leukemia studied by fluorescence in situ hybridization.  [electronic resource] 

 -  Cancer genetics and cytogenetics  Jun 1998 
 - 110-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0165-4608 
<br/><br/><label>Standard No.: </label>10.1016/s0165-4608(97)00410-x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Azure Stains--metabolism<br/>Centromere--genetics<br/>Chromosome Aberrations--genetics<br/>Chromosome Banding<br/>Chromosome Disorders<br/>Chromosomes, Human, Pair 11--genetics<br/>Chromosomes, Human, Pair 14--genetics<br/>Chromosomes, Human, Pair 8--genetics<br/>Female<br/>Genes, myc<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Karyotyping<br/>Leukemia, Prolymphocytic--genetics<br/>Leukemia, T-Cell--genetics<br/>Male<br/>Middle Aged<br/>X Chromosome--genetics