Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6|[sol]|RUNX1-rearranged childhood acute lymphoblastic leukaemia

A Attarbaschi; G Mann; S Strehl; M K?nig; M Steiner; V Jeitler; Th Lion; M N Dworzak; H Gadner; O A Haas

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Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6|[sol]|RUNX1-rearranged childhood acute lymphoblastic leukaemia

机译：缺失11q23是ETV6 | [sol] | RUNX1重排的儿童急性淋巴细胞白血病的高度特异性的非随机性继发遗传异常

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《Leukemia》 |2007年第5期|共1页
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A Attarbaschi; G Mann; S Strehl; M K?nig; M Steiner; V Jeitler; Th Lion; M N Dworzak; H Gadner; O A Haas;
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中图分类肿瘤学;
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1. Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6|[sol]|RUNX1-rearranged childhood acute lymphoblastic leukemia [J] . A Attarbaschi, G Mann, S Strehl, Leukemia . 2007,第3期

机译：缺失11q23是ETV6 | [sol] | RUNX1重排的儿童急性淋巴细胞白血病的高度特异性的非随机性继发遗传异常
2. Native ETV6 deletions accompanied by ETV6-RUNX1 rearrangements are associated with a favourable prognosis in childhood acute lymphoblastic leukaemia: a candidate for prognostic marker. [J] . Ko DH, Jeon Y, Kang HJ, British Journal of Haematology . 2011,第4期

机译：伴有ETV6-RUNX1重排的本地ETV6缺失与儿童急性淋巴细胞白血病（预后标志物的候选者）的良好预后相关。
3. Native ETV6 deletions accompanied by ETV6-RUNX1 rearrangements are associated with a favourable prognosis in childhood acute lymphoblastic leukaemia: a candidate for prognostic marker [J] . Dae-Hyun Ko, Yongbum Jeon, Hyoung Jin Kang, British Journal of Haematology . 2011,第4期

机译：伴有ETV6-RUNX1重排的本地ETV6缺失与儿童急性淋巴细胞白血病的良好预后相关：预后标志物的候选者
4. Research and Treatment of Childhood Acute Lymphoblastic Leukaemia [C] . . 2006

机译：儿童急性淋巴细胞白血病的研究与治疗
5. Deletion in 9q34 in abnormal karyotype (AK) precursor B adult acute lymphoblastic leukemia (B-ALL). [D] . Dharmadhikari, Avinash. 2010

机译：9q34中异常核型（AK）前体B成人急性淋巴细胞白血病（B-ALL）的缺失。
6. Evaluation of ETV6/RUNX1 Fusion and Additional Abnormalities Involving ETV6 and/or RUNX1 Genes Using FISH Technique in Patients with Childhood Acute Lymphoblastic Leukemia [O] . Cigdem Aydin, Zafer Cetin, Ayse Esra Manguoglu, 2016

机译：应用FISH技术评估儿童急性淋巴细胞白血病中ETV6 / RUNX1融合以及涉及ETV6和/或RUNX1基因的其他异常
7. Germline genetic variation in ETV6 and risk of childhood acute lymphoblastic leukaemia: a systematic genetic study [O] . Department of Pharmaceutical Sciences, St Jude Children's Research Hospital, Memphis, TN, USA ( host institution ), Moriyama, Takaya ( author ), Metzger, Monika L ( author ), 2015

机译：ETV6中的种系遗传变异与儿童急性淋巴细胞白血病的风险：系统的遗传研究

Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6|[sol]|RUNX1-rearranged childhood acute lymphoblastic leukaemia

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