Kajsa Paulsson
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- 2015
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Mark
The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013.
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- Contribution to journal › Article
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Mark
Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1.
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- Contribution to journal › Article
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Mark
A Population-Based Single Nucleotide Polymorphism Array Analysis of Genomic Aberrations in Younger Adult Acute Lymphoblastic Leukemia Patients
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- Contribution to journal › Article
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Mark
Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article
- 2014
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Mark
Deletions of IKZF1 and SPRED1 are associated with poor prognosis in a population-based series of pediatric B-cell precursor acute lymphoblastic leukemia diagnosed between 1992 and 2011.
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- Contribution to journal › Article
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Mark
Allelic variants of PRDM9 associated with high hyperdiploid childhood acute lymphoblastic leukaemia.
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- Contribution to journal › Letter
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Mark
Risk of RAS in relapsed childhood ALL.
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- Contribution to journal › Debate/Note/Editorial
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Mark
Comprehensive genetic characterization of pediatric T-cell acute lymphoblastic leukemia
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- Contribution to journal › Published meeting abstract
- 2013
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Mark
Partial 17q gain resulting from isochromosomes, unbalanced translocations, and complex rearrangements is associated with gene overexpression, older age, and shorter overall survival in high hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Letter
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Mark
Loss of chromosomes is the primary event in near-haploid and low hypodiploid acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols
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- Contribution to journal › Article
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Mark
Distinct patterns of gained chromosomes in high hyperdiploid acute lymphoblastic leukemia with t(1;19)(q23;p13), t(9;22)(q34;q22) or MLL rearrangements.
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- Contribution to journal › Letter
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Mark
Genomic Heterogeneity in Acute Leukemia.
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- Contribution to journal › Article
- 2012
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Mark
High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.
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- Contribution to journal › Article