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

Flach, Johanna; Shumilov, Evgenii; Joncourt, Raphael; Porret, Naomi; Tchinda, Joëlle; Legros, Myriam; Scarpelli, Ilaria; Hewer, Ekkehard; Novak, Urban; Schoumans, Jacqueline; Bacher, Vera; Pabst, Thomas (2020). Detection of rare reciprocal RUNX1 rearrangements by next‐generation sequencing (NGS) in acute myeloid leukemia. Genes, chromosomes & cancer, 59(4), pp. 268-274. Wiley 10.1002/gcc.22829

[img] Text
Flach_et_al-2019-Genes,_Chromosomes_and_Cancer.pdf - Published Version
Restricted to registered users only
Available under License Publisher holds Copyright.
Download (1MB)

Item Type:

 Journal Article (Original Article)

Division/Institute:

 04 Faculty of Medicine > Service Sector > Institute of Pathology > Cytopathology
04 Faculty of Medicine > Service Sector > Institute of Pathology > Clinical Pathology
04 Faculty of Medicine > Service Sector > Institute of Pathology
04 Faculty of Medicine > Department of Haematology, Oncology, Infectious Diseases, Laboratory Medicine and Hospital Pharmacy (DOLS) > Clinic of Haematology and Central Haematological Laboratory
04 Faculty of Medicine > Department of Haematology, Oncology, Infectious Diseases, Laboratory Medicine and Hospital Pharmacy (DOLS) > Clinic of Medical Oncology

UniBE Contributor:

 Joncourt, Raphael, Porret, Naomi, Legros, Myriam, Hewer, Ekkehard Walter, Novak, Urban, Bacher, Vera Ulrike, Pabst, Thomas Niklaus

Subjects:

 600 Technology > 610 Medicine & health
500 Science > 570 Life sciences; biology

ISSN:

 1098-2264

Publisher:

 Wiley

Language:

 English

Submitter:

 Ekkehard Hewer

Date Deposited:

 06 Dec 2019 15:54

Last Modified:

 02 Mar 2023 23:32

Publisher DOI:

 10.1002/gcc.22829

PubMed ID:

 31756777

BORIS DOI:

 10.7892/boris.135532

URI:

 https://boris.unibe.ch/id/eprint/135532

Actions (login required)

Edit item Edit item
Provide Feedback