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Interstitial deletion of 9q in a case of acute myeloid leukemia with t(8;21).伴有t(8;21)的急性髓系白血病病例中9号染色体长臂的间质缺失。
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2
Characterization of acute myeloid leukemia with del(9q) - Impact of the genes in the minimally deleted region.伴有9号染色体长臂缺失(del(9q))的急性髓系白血病的特征——最小缺失区域内基因的影响
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Interstitial 9q deletion is associated with CD7+ acute leukemia of myeloid and T lymphoid lineage.间质9号染色体缺失与髓系和T淋巴系CD7+急性白血病相关。
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本文引用的文献

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A simple, robust, validated and highly predictive index for the determination of risk-directed therapy in acute myeloid leukaemia derived from the MRC AML 10 trial. United Kingdom Medical Research Council's Adult and Childhood Leukaemia Working Parties.一种简单、可靠、经过验证且具有高度预测性的指数,用于确定源自医学研究理事会(MRC)AML 10试验的急性髓系白血病的风险导向治疗。英国医学研究理事会成人及儿童白血病工作组。
Br J Haematol. 1999 Oct;107(1):69-79. doi: 10.1046/j.1365-2141.1999.01684.x.
2
The importance of diagnostic cytogenetics on outcome in AML: analysis of 1,612 patients entered into the MRC AML 10 trial. The Medical Research Council Adult and Children's Leukaemia Working Parties.诊断细胞遗传学对急性髓系白血病预后的重要性:对参加医学研究委员会AML 10试验的1612例患者的分析。医学研究委员会成人及儿童白血病工作组。
Blood. 1998 Oct 1;92(7):2322-33.
3
Fifty-one patients with acute myeloid leukemia and translocation t(8;21)(q22;q22): an additional deletion in 9q is an adverse prognostic factor.51例急性髓系白血病伴t(8;21)(q22;q22)易位患者:9号染色体长臂额外缺失是不良预后因素。
Leukemia. 1996 Aug;10(8):1288-95.
4
Identificaton of a translocation with quinacrine fluorescence in a patient with acute leukemia.一名急性白血病患者中用喹吖因荧光法鉴定出一种易位。
Ann Genet. 1973 Jun;16(2):109-12.
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Acute myelogenous leukemia with an 8;21 translocation. A report on 148 cases from the Groupe Français de Cytogénétique Hématologique.伴有8号与21号染色体易位的急性髓系白血病。法国血液细胞遗传学小组关于148例病例的报告。
Cancer Genet Cytogenet. 1990 Feb;44(2):169-79.
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Prognostic importance of cytogenetic subgroups in de novo pediatric acute nonlymphocytic leukemia.
J Clin Oncol. 1990 Jan;8(1):75-83. doi: 10.1200/JCO.1990.8.1.75.

Interstitial deletion of 9q in a case of acute myeloid leukemia with t(8;21).

作者信息

Kar B, Dhanalakshmi K G, Revathi R

机构信息

Department of Medical Genetics, Department of Pediatric Hematology, Apollo Hospitals, Chennai, 600 006 India.

出版信息

Indian J Hematol Blood Transfus. 2008 Jun;24(2):75-7. doi: 10.1007/s12288-008-0034-7. Epub 2008 Aug 24.

DOI:10.1007/s12288-008-0034-7
PMID:23100950
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3453036/
Abstract
摘要