Shiba, Norio <br/><br/>
CBL mutation in chronic myelomonocytic leukemia secondary to familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML).  [electronic resource] 

 -  Blood  Mar 2012 
 - 2612-4 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-2011-02-333435  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Blood Platelet Disorders--complications<br/>Child<br/>Chromosomes, Human, Pair 11--genetics<br/>Core Binding Factor Alpha 2 Subunit--genetics<br/>Female<br/>Genes, Dominant<br/>Genetic Predisposition to Disease<br/>Haplotypes--genetics<br/>Humans<br/>Immunoblotting<br/>Leukemia, Myeloid, Acute--complications<br/>Leukemia, Myelomonocytic, Chronic--etiology<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Pedigree<br/>Polymerase Chain Reaction<br/>Proto-Oncogene Proteins c-cbl--genetics