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- 2007
-
Mark
The molecular signature of MDS stem cells supports a stem-cell origin of 5q - myelodysplastic syndromes
- Contribution to journal › Article
- 2006
-
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
Schoumans, Jacqueline ; Johansson, Bertil LU ; Corcoran, Martin ; Kuchinskaya, Ekaterina ; Golovleva, Irina ; Grander, Dan ; Forestier, Erik ; Staaf, Johan LU
; Borg, Åke
LU
and Gustafsson, Britt
, et al.
(2006)
In British Journal of Haematology
135(4).
p.492-499
- Contribution to journal › Article
-
Mark
Array-based comparative genomic hybridization characterization of cytogenetically polyclonal myeloid malignancies.
Davidsson, Josef LU
; Heidenblad, Markus
LU
; Borg, Åke
LU
and Johansson, Bertil
LU
(2006)
In Cancer Genetics and Cytogenetics
169(2).
p.179-180
- Contribution to journal › Letter
-
Mark
Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia.
Paulsson, Kajsa LU ; Heidenblad, Markus LU
; Mörse, Helena
LU
; Borg, Åke
LU
; Fioretos, Thoas
LU
and Johansson, Bertil
LU
(2006)
In Leukemia
20(11).
p.2002-2007
- Contribution to journal › Article
-
Mark
MLL/GAS7 fusion in a pediatric case of t(11;17)(q23;p13)-positive precursor B-cell acute lymphoblastic leukemia
Panagopoulos, Ioannis LU ; Lilljebjörn, Henrik LU
; Strömbeck, Bodil
LU
; Hjorth, Lars
LU
; Olofsson, Tor
LU
and Johansson, Bertil
LU
(2006)
In Haematologica
91(9).
p.1287-1288
- Contribution to journal › Letter
-
Mark
Antithymocyte globulin and cyclosporine A as combination therapy for low-risk non-sideroblastic myelodysplastic syndromes
- Contribution to journal › Article
-
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
Paulsson, Kajsa LU ; Békássy, Albert LU ; Olofsson, Tor LU ; Mitelman, Felix LU
; Johansson, Bertil
LU
and Panagopoulos, Ioannis
LU
(2006)
In Leukemia
20(2).
p.224-229
- Contribution to journal › Article
-
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.
Paulsson, Kajsa LU ; Heidenblad, Markus LU
; Strömbeck, Bodil
LU
; Staaf, Johan
LU
; Jönsson, Göran B
LU
; Borg, Åke
LU
; Fioretos, Thoas
LU
and Johansson, Bertil
LU
(2006)
In Leukemia
20(5).
p.840-846
- Contribution to journal › Article
-
Mark
Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias
Davidsson, Josef LU
; Paulsson, Kajsa
LU
and Johansson, Bertil
LU
(2006)
In European Journal of Haematology
76(5).
p.449-450
- Contribution to journal › Letter
-
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.
- Contribution to journal › Article