Magnani, I <br/><br/>
A recurrent 19q11-12 breakpoint suggested by cytogenetic and fluorescence in situ hybridization analysis of three glioblastoma cell lines.  [electronic resource] 

 -  Cancer genetics and cytogenetics  Apr 1999 
 - 82-6 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(98)00190-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Brain Neoplasms--genetics<br/>Chromosome Aberrations<br/>Chromosome Banding<br/>Chromosome Breakage<br/>Chromosomes, Human, Pair 19<br/>Glioblastoma--genetics<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Karyotyping<br/>Translocation, Genetic<br/>Tumor Cells, Cultured