Quentin, Samuel <br/><br/>
Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions.  [electronic resource] 

 -  Blood  Apr 2011 
 - e161-70 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-2010-09-308726  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Bone Marrow--physiology<br/>Child<br/>Child, Preschool<br/>Core Binding Factor Alpha 2 Subunit--genetics<br/>Fanconi Anemia--complications<br/>Female<br/>Gene Dosage--genetics<br/>Gene Expression Profiling<br/>Gene Expression Regulation, Leukemic<br/>Genes, Tumor Suppressor<br/>Genomic Instability--genetics<br/>Homozygote<br/>Humans<br/>Leukemia, Myeloid, Acute--etiology<br/>Male<br/>Middle Aged<br/>Myelodysplastic Syndromes--etiology<br/>Nucleophosmin<br/>Polymorphism, Single Nucleotide<br/>Young Adult