High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.

Kristina Karrman; Erik Forestier; Mette K Andersen; Kirsi Autio; Georg Borgstrom; Sverre Heim; Kristina Heinonen; Randi Hovland; Gitte Kerndrup; Bertil Johansson

doi:10.1111/j.1365-2141.2006.06286.x

High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.

Kristina Karrman, Erik Forestier, Mette K Andersen, Kirsi Autio, Georg Borgstrom, Sverre Heim, Kristina Heinonen, Randi Hovland, Gitte Kerndrup, Bertil Johansson

Division of Clinical Genetics

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	352-354
Journal	British Journal of Haematology
Volume	135
Issue number	3
DOIs	https://doi.org/10.1111/j.1365-2141.2006.06286.x
Publication status	Published - 2006

Subject classification (UKÄ)

Hematology

Access to Document

10.1111/j.1365-2141.2006.06286.x

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16965388&dopt=Abstract

Cite this

Karrman, K., Forestier, E., Andersen, M. K., Autio, K., Borgstrom, G., Heim, S., Heinonen, K., Hovland, R., Kerndrup, G., & Johansson, B. (2006). High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005. British Journal of Haematology, 135(3), 352-354. https://doi.org/10.1111/j.1365-2141.2006.06286.x

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title = "High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.",

author = "Kristina Karrman and Erik Forestier and Andersen, {Mette K} and Kirsi Autio and Georg Borgstrom and Sverre Heim and Kristina Heinonen and Randi Hovland and Gitte Kerndrup and Bertil Johansson",

year = "2006",

doi = "10.1111/j.1365-2141.2006.06286.x",

language = "English",

volume = "135",

pages = "352--354",

journal = "British Journal of Haematology",

issn = "0007-1048",

publisher = "Wiley-Blackwell",

number = "3",

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Karrman, K, Forestier, E, Andersen, MK, Autio, K, Borgstrom, G, Heim, S, Heinonen, K, Hovland, R, Kerndrup, G & Johansson, B 2006, 'High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.', British Journal of Haematology, vol. 135, no. 3, pp. 352-354. https://doi.org/10.1111/j.1365-2141.2006.06286.x

High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005. / Karrman, Kristina; Forestier, Erik; Andersen, Mette K et al.

In: British Journal of Haematology, Vol. 135, No. 3, 2006, p. 352-354.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.

AU - Karrman, Kristina

AU - Forestier, Erik

AU - Andersen, Mette K

AU - Autio, Kirsi

AU - Borgstrom, Georg

AU - Heim, Sverre

AU - Heinonen, Kristina

AU - Hovland, Randi

AU - Kerndrup, Gitte

AU - Johansson, Bertil

PY - 2006

Y1 - 2006

U2 - 10.1111/j.1365-2141.2006.06286.x

DO - 10.1111/j.1365-2141.2006.06286.x

M3 - Article

C2 - 16965388

VL - 135

SP - 352

EP - 354

JO - British Journal of Haematology

JF - British Journal of Haematology

SN - 0007-1048

IS - 3

ER -

Karrman K, Forestier E, Andersen MK, Autio K, Borgstrom G, Heim S et al. High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005. British Journal of Haematology. 2006;135(3):352-354. https://doi.org/10.1111/j.1365-2141.2006.06286.x