Kajsa Paulsson
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- 2010
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Mark
Molecular characterisation of a recurrent, semi-cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia
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- Contribution to journal › Article
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Mark
The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations.
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- Contribution to journal › Article
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Mark
Relapsed childhood high hyperdiploid acute lymphoblastic leukemia: presence of preleukemic ancestral clones and the secondary nature of microdeletions and RTK-RAS mutations.
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- Contribution to journal › Article
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Mark
Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article
- 2009
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Mark
Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia
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- Contribution to journal › Article
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Mark
Relapsed Childhood High Hyperdiploid Acute Lymphoblastic Leukemia: Genome-Wide Screening Reveals the Presence of Preleukemic Ancestral Clones and the Secondary Nature of Microdeletions and RTK-RAS Mutations
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- Contribution to journal › Published meeting abstract
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Mark
High hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article
- 2008
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Mark
Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease
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- Contribution to journal › Article
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Mark
Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia
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- Contribution to journal › Article
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Mark
FLT3 mutations in a 10 year consecutive series of 177 childhood acute leukemias and their impact on global gene expression patterns.
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- Contribution to journal › Article