Detection of rare reciprocal RUNX1 rearrangements by next‐generation sequencing in acute myeloid leukemia-Reference-Cited by-同舟云学术

Detection of rare reciprocal RUNX1 rearrangements by next‐generation sequencing in acute myeloid leukemia

Published:2019-12-02 Issue:4 Volume:59 Page:268-274
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Flach Johanna¹,Shumilov Evgenii²,Joncourt Raphael³,Porret Naomi³,Tchinda Joëlle⁴,Legros Myriam⁵,Scarpelli Ilaria⁶,Hewer Ekkehard⁷^ORCID,Novak Urban⁸,Schoumans Jacqueline⁶,Bacher Ulrike³⁵^ORCID,Pabst Thomas⁸

Affiliation:

1. Department of Hematology and Oncology Medical Faculty Mannheim of the Heidelberg University Mannheim Germany

2. Department of Hematology and Medical Oncology University Medicine Göttingen Göttingen Germany

3. University Department of Hematology and Central Hematology Laboratory Inselspital, Bern University Hospital Bern Switzerland

4. Oncology Laboratory University Children's Hospital Zurich Zurich Switzerland

5. Center of Laboratory Medicine (ZLM) Inselspital, Bern University Hospital Bern Switzerland

6. Department of Cancer Genetics, Laboratory Department CHUV, University of Lausanne Lausanne Switzerland

7. Institute of Pathology University of Bern Bern Switzerland

8. Department of Medical Oncology Inselspital, Bern University Hospital Bern Switzerland

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.22829

Reference25 articles.

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3. Detection of recurrent and of novel fusion transcripts in myeloid malignancies by targeted RNA sequencing

4. RNA-sequencing analysis of core binding factor AML identifies recurrent ZBTB7A mutations and defines RUNX1-CBFA2T3 fusion signature

5. Molecular Minimal Residual Disease in Acute Myeloid Leukemia

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