Patients with RUNX1 (AML1) amplification exhibit consistent genomic amplification, chromosome instability and a distinct gene expression signature.

被引：0
|
作者：
Strefford, J
Van Delft, F
Robinson, HM
Worley, H
Selzer, R
Young, BD
Saha, V
Harrison, CJ
机构：
[1] Univ Southampton, Canc Sci Div, Leukaemia Res Fund, Cytogenet Grp, Southampton SO9 5NH, Hants, England
[2] Univ London, Queen Mary, Canc Res UK Childrens Canc Grp, London WC1E 7HU, England
[3] NimbleGen Syst Inc, Madison, WI USA
[4] Univ London, Queen Mary, Canc Res UK Med Oncol Unit, London WC1E 7HU, England
来源：
JOURNAL OF MEDICAL GENETICS | 2005年 / 42卷
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D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
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页码：S65 / S65
页数：1
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