Molecular cytogenetic detection of the ASXL1 gene alterations in patients with 20q deletion

被引：0
|
作者：
Brezinova, Jana [1 ]
Sarova, Iveta [1 ]
Ransdorfova, Sarka [1 ]
Svobodova, Karla [2 ,3 ,4 ]
Lhotska, Halka [2 ,3 ,4 ]
Izakova, Silvia [2 ,3 ,4 ]
Pavlistova, Lenka [2 ,3 ,4 ]
Zemanova, Zuzana [2 ,3 ,4 ]
Markova, Jana [5 ]
Cermak, Jaroslav [6 ]
Jonasova, Anna [7 ,8 ]
Michalova, Kyra [2 ,3 ,4 ]
机构：
[1] Inst Hematol & Blood Transfus, Dept Cytogenet, Prague, Czech Republic
[2] Charles Univ Prague, Ctr Oncocytogenet, Inst Med Biochem, Prague, Czech Republic
[3] Charles Univ Prague, Ctr Oncocytogenet, Lab Diagnost, Gen Univ Hosp, Prague, Czech Republic
[4] Charles Univ Prague, Ctr Oncocytogenet, Fac Med 1, Prague, Czech Republic
[5] Inst Hematol & Blood Transfus, Dept Mol Genet, Prague, Czech Republic
[6] Inst Hematol & Blood Transfus, Clin Dept, Prague, Czech Republic
[7] Charles Univ Prague, Med Dept 1, Gen Univ Hosp, Prague, Czech Republic
[8] Charles Univ Prague, Med Dept 1, Fac Med 1, Prague, Czech Republic
来源：
MOLECULAR CYTOGENETICS | 2017年 / 10卷
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
2.P5
引用
收藏
页数：2
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