Zong, Xiangping <br/><br/>
ASXL1 mutations are frequent in de novo AML with trisomy 8 and confer an unfavorable prognosis.  [electronic resource] 

 -  Leukemia & lymphoma  01 2017 
 - 204-206 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>1029-2403 
<br/><br/><label>Standard No.: </label>10.1080/10428194.2016.1179296  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acute Disease<br/>Adolescent<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Child<br/>Chromosomes, Human, Pair 8--genetics<br/>Female<br/>Humans<br/>Kaplan-Meier Estimate<br/>Leukemia, Myeloid--genetics<br/>Male<br/>Middle Aged<br/>Mutation<br/>Prognosis<br/>Repressor Proteins--genetics<br/>Trisomy--genetics<br/>Young Adult