Genome-wide genotyping of acute myeloid leukemia with translocation t(9;11)(p22;q23) reveals novel recurrent genomic alterations

被引：6
|
作者：
Kuehn, Michael W. M. [1 ]
Bullinger, Lars [1 ]
Groeschel, Stefan [1 ]
Kroenke, Jan [1 ]
Edelmann, Jennifer [1 ]
Ruecker, Frank G. [1 ]
Eiwen, Karina [1 ]
Paschka, Peter [1 ]
Gaidzik, Verena I. [1 ]
Holzmann, Karlheinz [2 ]
Schlenk, Richard F. [1 ]
Doehner, Hartmut [1 ]
Doehner, Konstanze [1 ]
机构：
[1] Univ Ulm, Dept Internal Med 3, D-89069 Ulm, Germany
[2] Univ Ulm, Microarray Core Facil, D-89069 Ulm, Germany
来源：
HAEMATOLOGICA | 2014年 / 99卷 / 08期
关键词：
acute myeloid leukemia; copy number alterations; genotyping; t(9; 11)(p22; q23); novel recurrent genomic alterations; GENE;
D O I：
10.3324/haematol.2014.105544
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：E133 / E135
页数：3
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