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- 2015
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Mark
Cancer cytogenetics : Chromosomal and Molecular Genetic Aberrations of Tumor Cells
Heim, Sverre LU and Mitelman, Felix LU (2015)
- Book/Report › Anthology (editor)
-
Mark
Preface to the Fourth Edition
2015)(
- Chapter in Book/Report/Conference proceeding › Foreword/Postscript
-
Mark
How it all began : Cancer cytogenetics before sequencing
2015) p.1-10(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Cytogenetic nomenclature
2015) p.19-25(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Nonrandom chromosome abnormalities in cancer : An overview
2015) p.26-41(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Tumors of the skin
2015) p.555-565(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2014
-
Mark
Sequencing IDH1/2 glioma mutation hotspots in gliomas and malignant peripheral nerve sheath tumors.
(
- Contribution to journal › Letter
-
Mark
Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries
(
- Contribution to journal › Article
- 2013
-
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
(
- Contribution to journal › Article
- 2012
-
Mark
Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol
(
- Contribution to journal › Letter
- 2011
-
Mark
Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols.
(
- Contribution to journal › Article
- 2009
-
Mark
t(19;22)(q13;q12) Translocation Leading to the Novel Fusion Gene EWSRI-ZNF444 in Soft Tissue Myoepithelial Carcinoma
(
- Contribution to journal › Article
-
Mark
t(3;21)(q22;q22) leading to truncation of the RYK gene in atypical chronic myeloid leukemia
(
- Contribution to journal › Article
-
Mark
Cytogenetic Analysis of 101 Giant Cell Tumors of Bone: Nonrandom Patterns of Telomeric Associations and Other Structural Aberrations
(
- Contribution to journal › Article
-
Mark
Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: Rare T-cell receptor gene rearrangements are associated with poor outcome.
(
- Contribution to journal › Article
- 2008
-
Mark
Molecular screening for new fusion genes in cancer
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Detection of a t(1;22)(q23;q 12) translocation leading to an EWSR1-PBX1 fusion gene in a myoepithelioma
(
- Contribution to journal › Article
-
Mark
Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival
(
- Contribution to journal › Article
-
Mark
Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-Cell precursor acute lymphoblastic leukemias: A nordic series of 24 cases and review of the literature
(
- Contribution to journal › Scientific review
- 2007
-
Mark
Molecular cytogenetic characterization of t(14;19)(q32;p13), a new recurrent translocation in B cell malignancies
(
- Contribution to journal › Article
-
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
(
- Contribution to journal › Scientific review
- 2006
-
Mark
Deregulation of HMGA2 in an aggressive angiomyxoma with t(11;12)(q23;q15)
(
- Contribution to journal › Article
-
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
- 2004
-
Mark
Tumor karyotype predicts clinical outcome in colorectal cancer patients
(
- Contribution to journal › Article
- 2003
-
Mark
Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas
(
- Contribution to journal › Article
-
Mark
Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001.
(
- Contribution to journal › Article
- 2002
-
Mark
Chromosomal aberrations in benign and malignant Bilharzia-associated bladder lesions analyzed by comparative genomic hybridization.
(
- Contribution to journal › Article
-
Mark
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.
(
- Contribution to journal › Article
- 2001
-
Mark
Identification of cytogenetic subgroups and karyotypic pathways in transitional cell carcinoma
(
- Contribution to journal › Article
-
Mark
Characterization of chromosomal abnormalities in uroepithelial carcinomas by G-banding, spectral karyotyping and fish analysis
(
- Contribution to journal › Article
- 1996
-
Mark
t(3;21)(q26;q22) with AML1 rearrangement in a de novo childhood acute monoblastic leukaemia
(
- Contribution to journal › Article
- 1994
-
Mark
Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22)
(
- Contribution to journal › Article
- 1993
-
Mark
Comparative cytogenetic and DNA flow cytometric analysis of 150 bone and soft-tissue tumors
(
- Contribution to journal › Article
-
Mark
Clinical impact of breakpoint position within M-bcr in chronic myeloid leukemia
(
- Contribution to journal › Article
- 1992
-
Mark
Molecular analysis of Philadelphia-positive childhood chronic myeloid leukemia.
(
- Contribution to journal › Article
-
Mark
Acute myelomonocytic leukemia with inv(16)(p13q22) complicating Philadelphia chromosome positive chronic myeloid leukemia
(
- Contribution to journal › Article
-
Mark
Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11)
(
- Contribution to journal › Article
-
Mark
Chromosome aberrations in 35 primary ovarian carcinomas
(
- Contribution to journal › Article
- 1991
-
Mark
New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia
(
- Contribution to journal › Article
- 1990
-
Mark
Deletion of 14q in non‐Hodgkin's lymphoma
(
- Contribution to journal › Article
-
Mark
Localization of the chromosomal breakpoints of the t(12;16) in liposarcoma to subbands 12q13.3 and 16p11.2
(
- Contribution to journal › Article
-
Mark
Bone marrow karyotypes in 94 children with acute leukemia
(
- Contribution to journal › Article
-
Mark
Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas
(
- Contribution to journal › Article
-
Mark
Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement
(
- Contribution to journal › Article
- 1989
-
Mark
Complex karyotypic anomalies in a bizarre leiomyoma of the uterus.
(
- Contribution to journal › Article
-
Mark
Characteristic karyotypic anomalies identify subtypes of malignant fibrous histiocytoma
(
- Contribution to journal › Article
-
Mark
No abnormal C‐band polymorphism in lung cancer patients
(
- Contribution to journal › Article
- 1988
-
Mark
Do clonal chromosome abnormalities prognosticate early relapse in hodgkin's disease?
(
- Contribution to journal › Letter
-
Mark
Trisomy 5 and t(5;14)(q11;q32) as the sole abnormalities in two different clones from a centroblastic non-Hodgkin's lymphoma
(
- Contribution to journal › Article
-
Mark
Normal frequency of structural chromosome aberrations in fibroblasts from patients with non‐Hodgkin's lymphoma
(
- Contribution to journal › Article
-
Mark
Breakprone chromosome bands in fibroblasts from patients with non‐Hodgkin's lymphoma do not coincide with bands involved in primary rearrangements in non‐Hodgkin's lymphomas
(
- Contribution to journal › Article
- 1987
-
Mark
RELATIONSHIP BETWEEN CYTOGENETIC FINDINGS AND HISTOPATHOLOGY IN NON‐HODGKIN LYMPHOMA
(
- Contribution to journal › Article
-
Mark
CYTOGENETIC STUDIES IN HODGKIN'S DISEASE
(
- Contribution to journal › Article
-
Mark
Prognostic implication of cytogenetic findings in 106 patients with non-Hodgkin lymphoma
(
- Contribution to journal › Article
-
Mark
New structural chromosomal rearrangements in congenital leukemia
(
- Contribution to journal › Article
-
Mark
A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia
(
- Contribution to journal › Article
- 1986
-
Mark
Cytogenetic studies in non‐Hodgkin lymphomas ‐ Results from surgical biopsies
(
- Contribution to journal › Article
-
Mark
High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia
(
- Contribution to journal › Article
-
Mark
Reciprocal translocation (11;19)(q23;p13) in congenital acute lymphoblastic leukemia
(
- Contribution to journal › Article