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

页码：E133 / E135

页数：3

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