Kajsa Paulsson
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- 2007
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Mark
Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3
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- Contribution to journal › Article
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Mark
Characterisation of genomic translocation breakpoints and identification of an alternative TCF3/PBX1 fusion transcript in t(1;19)(q23;p13)-positive acute lymphoblastic leukaemias.
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- Contribution to journal › Article
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Mark
Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes.
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- Contribution to journal › Scientific review
- 2006
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Mark
Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias
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- Contribution to journal › Letter
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Mark
A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42
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- Contribution to journal › Article
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Mark
Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration.
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- Contribution to journal › Article
- 2005
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Mark
The parental origin of trisomy 14 in hyperdiploid childhood ALL
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- Contribution to journal › Letter
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Mark
Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article