Sinclair, E J <br/><br/>
Fluorescence in situ hybridization analysis of 25 cases of idiopathic myelofibrosis and two cases of secondary myelofibrosis: monoallelic loss of RB1, D13S319 and D13S25 loci associated with cytogenetic deletion and translocation involving 13q14.  [electronic resource] 

 -  British journal of haematology  May 2001 
 - 365-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0007-1048 
<br/><br/><label>Standard No.: </label>10.1046/j.1365-2141.2001.02754.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Chromosome Aberrations--diagnosis<br/>Chromosome Disorders<br/>Chromosomes, Human, Pair 13<br/>Female<br/>Gene Deletion<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Male<br/>Middle Aged<br/>Primary Myelofibrosis--genetics<br/>Translocation, Genetic