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2024
Mark How to manage patients with germline DDX41 variants : Recommendations from the Nordic working group on germline predisposition for myeloid neoplasms
Baliakas, Panagiotis ; Tesi, Bianca ; Cammenga, Jörg ^LU ; Stray-Pedersen, Asbjørg ; Jahnukainen, Kirsi ; Andersen, Mette Klarskov ; Ågerstam, Helena ^LU ; Creignou, Maria ; Dybedal, Ingunn and Raaschou-Jensen, Klas , et al. (2024) In HemaSphere 8(8).
- Contribution to journal › Article
2014
Mark Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries
Lundin, Catarina ^LU ; Forestier, Erik ; Andersen, Mette Klarskov ; Autio, Kirsi ; Barbany, Gisela ; Cavelier, Lucia ; Golovleva, Irina ; Heim, Sverre ; Heinonen, Kristiina and Hovland, Randi , et al. (2014) In Journal of Hematology & Oncology 7.
- Contribution to journal › Article
2012
Mark High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.
Lundin, Catarina ^LU ; Hjorth, Lars ^LU ; Behrendtz, Mikael ; Nordgren, Ann ; Palmqvist, Lars ; Andersen, Mette Klarskov ; Biloglav, Andrea ^LU ; Forestier, Erik ; Paulsson, Kajsa ^LU and Johansson, Bertil ^LU (2012) In Genes, Chromosomes and Cancer 51. p.196-206
- Contribution to journal › Article
2003
Mark Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001.
Forestier, Erik ; Heim, Sverre ; Blennow, Elisabeth ; Borgström, Georg ; Holmgren, Gösta ; Heinonen, Kristiina ; Johannsson, Johann ; Kerndrup, Gitte ; Andersen, Mette Klarskov and Lundin, Catarina , et al. (2003) In British Journal of Haematology 121(4). p.566-577
- Contribution to journal › Article

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