Submicroscopic Deletion of <i>RUNX1T1</i> Gene Confirmed by High-Resolution Microarray in Acute Myeloid Leukemia with <i>RUNX1/RUNX1T1</i> Rearrangement-Reference-Cited by-同舟云学术

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Submicroscopic Deletion of RUNX1T1 Gene Confirmed by High-Resolution Microarray in Acute Myeloid Leukemia with RUNX1/RUNX1T1 Rearrangement

Published:2012 Issue:1 Volume:127 Page:43-46
ISSN:1421-9662
Container-title:Acta Haematologica
language:en
Short-container-title:Acta Haematol

Author:

Yang John Jeongseok,Oh Seung Hwan,Cho Sun Young,Suh Jin-Tae,Lee Hee Joo,Lee Woo-In,Lee Juhie,Baek Sun Kyung,Yoon Hwi-Joong,Cho Eun Hae,Park Tae Sung

Publisher

S. Karger AG

Subject

Hematology,General Medicine

Reference9 articles.

1. Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis

2. Incidence of submicroscopic deletions vary according to disease entities and chromosomal translocations in hematologic malignancies: investigation by fluorescence in situ hybridization

3. Clinical Utility of Fluorescence in-situ Hybridization Profile Test in Detecting Genetic Aberrations in Acute Leukemia

4. Large deletions 5′ to the ETO breakpoint are recurrent events in patients with t(8;21) acute myeloid leukemia

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Acute promyelocytic leukemia with a STAT5b-RARα fusion transcript defined by array-CGH, FISH, and RT-PCR;Cancer Genetics;2012-06

2. Submicroscopic Deletion of FGFR1 Gene Is Recurrently Detected in Myeloid and Lymphoid Neoplasms Associated with ZMYM2-FGFR1 Rearrangements: A Case Study;Acta Haematologica;2012

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