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Leukemia & Lymphoma Volume 59, 2018 - Issue 12
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Letter to the Editor

Case studies investigating genetic heterogeneity between anatomically distinct bone marrow compartments in acute myeloid leukemia

Poojitha N. OjamiesInstitute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland; Correspondence[email protected]
ORCID Iconhttp://orcid.org/0000-0002-4921-7134View further author information
ORCID Icon,
Mika KontroHematology Research Unit Helsinki, University of Helsinki and Helsinki University Hospital Comprehensive Cancer Center, Helsinki, Finland; View further author information
,
Henrik EdgrenMediSapiens Ltd, Helsinki, Finland; View further author information
,
Pekka EllonenInstitute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland; View further author information
,
Caroline HeckmanInstitute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland; View further author information
,
Kimmo PorkkaHematology Research Unit Helsinki, University of Helsinki and Helsinki University Hospital Comprehensive Cancer Center, Helsinki, Finland; View further author information
,
Maija WolfInstitute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland; View further author information
&
Olli KallioniemiInstitute for Molecular Medicine Finland, FIMM, University of Helsinki, Helsinki, Finland; ;Science for Life Laboratory, Department of Oncology and Pathology, Karolinska Institutet, Solna, SwedenView further author information
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Pages 3002-3005 | Received 17 Feb 2018, Accepted 12 Mar 2018, Published online: 04 Apr 2018
 
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Acknowledgments

The authors are grateful to the patients for donating their samples for research. Kirsi Autio (HUSLAB, Helsinki, Finland) and Tuija Lundan (TYKSLAB, Turku, Finland) are thanked for providing sample materials from clinical specimens. FIMM Sequencing Lab (Maija Lepistö, Tiina Hannunen, Suvi Kyttänen, Sari Hannula and Aino Palva) are thanked for performing exome and amplicon sequencing experiments. Bioinformatics unit (Henrikki Almusa, Samuli Eldfors and Timo Miettinen) are thanked for executing the exome sequencing and amplicon pipelines.

Potential conflict of interest

Disclosure forms provided by the authors are available with the full text of this article online at https://doi.org/10.1080/10428194.2018.1453067.

Additional information

Funding

The research leading to these results were supported by Academy of Finland (Center of Excellence for Translational Cancer Biology), Cancer Society of Finland, Sigrid Juselius Foundation and TEKES, Syöpäjärjestöt and Terveyden Tutkimuksen Toimikunta.

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