MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies

被引：46

作者：

Ripperger, Tim ^{[1
]}

Hofmann, Winfried ^{[1
]}

Koch, Jan C. ^{[2
]}

Shirneshan, Katayoon ^{[1
,3
]}

Haase, Detlef ^{[3
]}

Wulf, Gerald ^{[3
]}

Issing, Peter R. ^{[4
]}

Karnebogen, Matthias ^{[5
]}

Schmidt, Gunnar ^{[1
]}

Auber, Bernd ^{[1
]}

Schlegelberger, Brigitte ^{[1
]}

Illig, Thomas ^{[1
,6
]}

Zirn, Birgit ^{[7
]}

Steinemann, Doris ^{[1
]}

机构：

[1] Hannover Med Sch, Dept Human Genet, Hannover, Germany

[2] Univ Med Ctr, Dept Neurol, Gottingen, Germany

[3] Georg August Univ, Dept Hematol & Oncol, Gottingen, Germany

[4] Klinikum Bad Hersfeld, Dept Otorhinolaryngol Head Neck & Facial Plast Su, Bad Hersfeld, Germany

[5] Healthpk Lenglern, Div Surg & Orthoped, Bovenden, Germany

[6] Hannover Med Sch, Hannover Unified Biobank, Hannover, Germany

[7] Genetikum, Genet Counseling & Diagnost, Stuttgart, Germany

来源：

HAEMATOLOGICA | 2018年 / 103卷 / 02期

关键词：

AMEGAKARYOCYTIC THROMBOCYTOPENIA; CONGENITAL THROMBOCYTOPENIA; RADIOULNAR SYNOSTOSIS; DNA; LEUKEMIA; MUTATION; FINGERS; PROTEIN; NEONATE; CELLS;

D O I：

10.3324/haematol.2017.178723

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：E55 / E58

页数：4

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