Fazi, Claudia <br/><br/>
General population low-count CLL-like MBL persists over time without clinical progression, although carrying the same cytogenetic abnormalities of CLL.  [electronic resource] 

 -  Blood  Dec 2011 
 - 6618-25 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1528-0020 
<br/><br/><label>Standard No.: </label>10.1182/blood-2011-05-357251  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>B-Lymphocytes--metabolism<br/>Chromosome Aberrations<br/>Chromosomes, Human, Pair 12--genetics<br/>Chromosomes, Human, Pair 13--genetics<br/>Chromosomes, Human, Pair 17--genetics<br/>Disease Progression<br/>Female<br/>Flow Cytometry<br/>Follow-Up Studies<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Leukemia, Lymphocytic, Chronic, B-Cell--diagnosis<br/>Lymphocyte Count<br/>Lymphocytosis--diagnosis<br/>Male<br/>Middle Aged<br/>Receptors, Antigen, T-Cell, alpha-beta--metabolism<br/>T-Lymphocytes--metabolism<br/>V(D)J Recombination--genetics