Bertil Johansson
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- 2007
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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
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Mark
Microarray-based classification of a consecutive series of 121 childhood acute leukemias: prediction of leukemic and genetic subtype as well as of minimal residual disease status.
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- Contribution to journal › Article
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Mark
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature
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- Contribution to journal › Scientific review
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Mark
Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region
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- Contribution to journal › Article
- 2006
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Mark
Fusion of ETV6 with an intronic sequence of the BAZ2A gene in a paediatric pre-B acute lymphoblastic leukaemia with a cryptic chromosome 12 rearrangement.
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- Contribution to journal › Article
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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
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.
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- Contribution to journal › Article
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Mark
FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2 : implications for formation and pathogenetic outcome of the idic(7)(p11.2)
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- Contribution to journal › Article
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Mark
Deregulation of cyclin D2 by juxtaposition with T-cell receptor alpha/delta locus in t(12;14)(p13;q11)-positive childhood T-cell acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene
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- Contribution to journal › Article
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Mark
Trisomy 19 as the sole chromosomal abnormality in proliferative chronic myelomonocytic leukemia
2006) In Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis 30(8). p.1043-1047(
- Contribution to journal › Article
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Mark
Array-based comparative genomic hybridization characterization of cytogenetically polyclonal myeloid malignancies.
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- Contribution to journal › Letter
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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
MLL/GAS7 fusion in a pediatric case of t(11;17)(q23;p13)-positive precursor B-cell acute lymphoblastic leukemia
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- Contribution to journal › Letter
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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
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Mark
Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2
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- Contribution to journal › Article
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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
Antithymocyte globulin and cyclosporine A as combination therapy for low-risk non-sideroblastic myelodysplastic syndromes
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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