Cryptic t(15;17) in a patient with AML M3 and a complex karyotype. - Suppr | 超能文献

Cryptic t(15;17) in a patient with AML M3 and a complex karyotype.

作者信息

Göhring Gudrun, Lange K, Atta J, Krauter J, Hölzer D, Schlegelberger B

出版信息

Cancer Genet Cytogenet. 2007 May;175(1):77-80. doi: 10.1016/j.cancergencyto.2007.01.004.

DOI:10.1016/j.cancergencyto.2007.01.004

Abstract

摘要

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Cryptic t(15;17) in a patient with AML M3 and a complex karyotype.

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Cryptic insertion (15;17) in a case of acute promyelocytic leukemia detected by fluorescence in situ hybridization.通过荧光原位杂交检测到的一例急性早幼粒细胞白血病中的隐匿性插入（15；17）。

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A t(17;20)(q21;q12) masking a variant t(15;17)(q22;q21) in a patient with acute promyelocytic leukemia.一名急性早幼粒细胞白血病患者中掩盖了变异型t(15;17)(q22;q21)的t(17;20)(q21;q12) 。

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Therapy-related acute myeloid leukemia after successful therapy for acute promyelocytic leukemia with t(15;17): A case report and literature review.急性早幼粒细胞白血病伴t(15;17)成功治疗后发生的治疗相关急性髓系白血病：一例报告并文献复习

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[Detection of PML/RARA rearrangement by reverse transcriptase-PCR and sequencing in a case of microgranular acute promyelocytic leukemia lacking t(15;17) on karyotype and FISH].[通过逆转录聚合酶链反应和测序检测一例核型和荧光原位杂交缺乏t(15;17)的微颗粒急性早幼粒细胞白血病中的PML/RARA重排]

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A new complex translocation t(5;17;15)(q11;q21;q22) in acute promyelocytic leukemia.急性早幼粒细胞白血病中的一种新的复杂易位t(5;17;15)(q11;q21;q22)

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Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion.变异型急性早幼粒细胞白血病15；17易位，起源于涉及相同15号和17号染色体的两个连续平衡易位，同时保留PML/RARA融合基因。

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[Detection of t(15;17) using cytogenetic, fluorescent in situ hybridization, and molecular techniques. Comparative study of 11 patients with acute promyelocytic leukemia].

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