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

页数：2

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