Myelodysplastic Syndromes (MDS) With 20q Deletion Show a High Frequency Of Associated Cytogenetic and Molecular Lesions With An Association To U2AF1, SRSF2, and Prognostically Adverse ASXL1 Mutations

被引：0
|
作者：
Bacher, Ulrike
Haferlach, Torsten
Schnittger, Susanne
Zenger, Melanie
Meggendorfer, Manja
Roller, Andreas
Grossmann, Vera
Krauth, Maria Theresa
Jeromin, Sabine
Alpermann, Tamara
Kohlmann, Alexander
Kern, Wolfgang
Haferlach, Claudia
机构：
来源：
BLOOD | 2013年 / 122卷 / 21期
关键词：
D O I：
10.1182/blood.V122.21.657.657
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
657
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页数：2
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