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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