Division of Clinical Genetics
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- 2004
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Mark
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients.
(
- Contribution to journal › Article
-
Mark
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
(
- Contribution to journal › Article
-
Mark
Reduced high-frequency QRS components in patients with ischemic heart disease compared to normal subjects
(
- Contribution to journal › Article
-
Mark
An excess of chromosome 1 breakpoints in male infertility.
(
- Contribution to journal › Article
-
Mark
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
(
- Contribution to journal › Article
-
Mark
Wilms tumors develop through two distinct karyotypic pathways.
(
- Contribution to journal › Article
-
Mark
Genome characteristics of primary carcinomas, local recurrences, carcinomatoses, and liver metastases from colorectal cancer patients
(
- Contribution to journal › Article
-
Mark
Establishment and phenotypic characterization of human U937 cells with inducible P210 BCR/ABL expression reveals upregulation of CEACAM1 (CD66a).
(
- Contribution to journal › Article
-
Mark
Sudanesiska cytogenetiker - vision om en ny form av bistånd
(
- Contribution to journal › Article
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Mark
Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.
(
- Contribution to journal › Article
-
Mark
Statistical dissection of cytogenetic patterns in lung cancer reveals multiple modes of karyotypic evolution independent of histological classification.
(
- Contribution to journal › Article
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Mark
Sequential cytogenetic and molecular cytogenetic characterization of an SV40T-immortalized nasopharyngeal cell line transformed by Epstein-Barr virus latent membrane protein-1 gene
(
- Contribution to journal › Article
-
Mark
The need for oncogenetic counselling - Ten years' experience of a regional oncogenetic clinic
(
- Contribution to journal › Article
-
Mark
Comparison of signal quality between EASI and Mason-Likar 12-lead electrocardiograms during physical activity.
(
- Contribution to journal › Article
-
Mark
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer
(
- Contribution to journal › Article
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Mark
Mitotic instability associated with late genomic changes in bone and soft tissue tumours.
(
- Contribution to journal › Article
-
Mark
Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma
(
- Contribution to journal › Article
-
Mark
Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.
(
- Contribution to journal › Article
-
Mark
External quality assessment for mutation detection in the BRCA1 and BRCA2 genes: EMQN's experience of 3 years
(
- Contribution to journal › Article
-
Mark
Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12).
(
- Contribution to journal › Article
-
Mark
Cytogenetic and fluorescence in situ hybridization characterization of clonal chromosomal aberrations and CCND1 amplification in esophageal carcinomas
(
- Contribution to journal › Article
-
Mark
Studies on Molecular Genetics of B cell Development
2004)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic characterization of bone and soft tissue tumors
(
- Contribution to journal › Article
-
Mark
Characterization of Genetic Abnormalities at Disease Progression of Chronic Myeloid Leukemia
2004)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Expression of DOL54 is not restricted to myxoid liposarcomas with the FUS-DDIT3 chimera but is found in various sarcomas.1
(
- Contribution to journal › Article
-
Mark
Genetic analyses of multiple myeloma and related plasma cell dyscrasias
2004)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetisk rådgivning och fosterdiagnostik.
2004) p.56-56(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Molecular Characterization of Genomic Amplifications in Pancreatic Cancer
2004)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Regulation of genetic testing in clinical practice
(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2003
-
Mark
Population genetic screening programmes: technical, social, and ethical issues.
(
- Contribution to journal › Article
-
Mark
Provision of genetic services in Europe: current practices and issues
(
- Contribution to journal › Article
-
Mark
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
The relative accuracies of ECG precordial lead waveforms derived from EASI leads and those acquired from paramedic applied standard leads
(
- Contribution to journal › Article
-
Mark
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma
(
- Contribution to journal › Article
-
Mark
Clinical and genetic studies of ETV6/ABL1-positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylate.
(
- Contribution to journal › Article
-
Mark
Genetic information and testing insurance and employment: technical, social, and ethical issues.
(
- Contribution to journal › Article
-
Mark
Prevalence of hemochromatosis gene (HFE) mutations in Greece
(
- Contribution to journal › Article
-
Mark
Cytogenetic and morphologic subgroups of myelodysplastic syndromes in relation to occupational and hobby exposures.
(
- Contribution to journal › Article
-
Mark
A pooled analysis of karyotypic patterns, breakpoints and imbalances in 783 cytogenetically abnormal multiple myelomas reveals frequently involved chromosome segments as well as significant age- and sex-related differences.
(
- Contribution to journal › Article
-
Mark
A novel fusion gene, SS18L1/SSX1, in synovial sarcoma
(
- Contribution to journal › Article
-
Mark
Ring Y chromosome in an azoospermic male with short stature: additional evidence for a distinct ring Y syndrome in non-mosaic patients?
(
- Contribution to journal › Letter
-
Mark
Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors
(
- Contribution to journal › Article
-
Mark
RNA analysis of B cell lines arrested at defined stages of differentiation allows for an approximation of gene expression patterns during B cell development.
(
- Contribution to journal › Article
-
Mark
Reduced proliferative capacity of hematopoietic stem cells deficient in hoxb3 and hoxb4.
(
- Contribution to journal › Article
-
Mark
Genomic characterization of MOZ/CBP and CBP/MOZ chimeras in acute myeloid leukemia suggests the involvement of a damage-repair mechanism in the origin of the t(8;16)(p11;p13).
(
- Contribution to journal › Article
-
Mark
Characterization of a novel breast carcinoma xenograft and cell line derived from a BRCA1 germ-line mutation carrier
(
- 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
-
Mark
Topoisomerase-II alpha is upregulated in malignant peripheral nerve sheath tumors and associated with clinical outcome
(
- Contribution to journal › Article
-
Mark
Consequences of eliminating adenosine A(1) receptors in mice
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
-
Mark
Provision of genetic service in Europe: current practices and issues.
(
- Contribution to journal › Article
-
Mark
Genetic profiling of colorectal cancer liver metastases by combined comparative genomic hybridization and G-banding analysis
(
- Contribution to journal › Article
-
Mark
Vitamin d receptor is expressed in pancreatic cancer cells and a vitamin d(3) analogue decreases cell number.
(
- Contribution to journal › Article
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Mark
Pancreatic carcinoma cell lines with SMAD4 inactivation show distinct expression responses to TGFB1.
(
- Contribution to journal › Article
-
Mark
Data storage and DNA banking for biomedical research: technical, social and ethical issues.
(
- Contribution to journal › Article
-
Mark
Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13).
(
- Contribution to journal › Article
-
Mark
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1
(
- Contribution to journal › Published meeting abstract
-
Mark
Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas
(
- Contribution to journal › Article
-
Mark
Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies. a multicolor and locus-specific fluorescence in situ hybridization study.
(
- Contribution to journal › Article
-
Mark
Fusion, disruption, and expression of HMGA2 in bone and soft tissue chondromas
(
- Contribution to journal › Article
-
Mark
Statens medicinsk-etiska råd. Genetisk screening - om hälsa och ärftlig sjukdomsrisk. Etiska vägmärken 11. (rec)
(
- Contribution to journal › Article
-
Mark
Power law distribution of chromosome aberrations in cancer.
(
- Contribution to journal › Article
-
Mark
Ett etiskt dilemma: Farmakogenetiskt test kan ge oönskad information [An ethical dilemma: pharmacogenetic tests can yield unwanted information]
(
- Contribution to journal › Article
-
Mark
Extraskeletal myxoid chondrosarcoma with neuroendocrine differentiation: a case report with fine-needle aspiration biopsy, histopathology, electron microscopy, and cytogenetics.
(
- Contribution to journal › Article
-
Mark
MYC is not overexpressed in a case of chronic myelomonocytic leukemia with MYC-containing double minutes
(
- Contribution to journal › Letter
-
Mark
Book review: P.J. Morrison, S.V. Hodgson, N.E. Haites (eds): Familial breast cancer: genetics, screening and managementCambridge University Press, 2002, 401 pp, hardcover (ISBN 0-521-80373-X) pound 65.00.
(
- Contribution to journal › Article
-
Mark
Cytogenetic findings and clinical course in a consecutive series of Wilms tumors
(
- Contribution to journal › Article
-
Mark
Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia
(
- Contribution to journal › Article
-
Mark
A Novel Gene, MSI2, Encoding a Putative RNA-binding Protein Is Recurrently Rearranged at Disease Progression of Chronic Myeloid Leukemia and Forms a Fusion Gene with HOXA9 as a Result of the Cryptic t(7;17)(p15;q23).
(
- Contribution to journal › Article
-
Mark
Lundensisk allvarshumor
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
-
Mark
Ovarian Carcinoma Develops through Multiple Modes of Chromosomal Evolution.
(
- Contribution to journal › Article
-
Mark
Chromosome instability in cancer: how, when, and why?
(
- Contribution to journal › Scientific review
-
Mark
Chromosomal abnormalities in inflammatory pseudotumor of the urinary bladder
(
- Contribution to journal › Article
-
Mark
Gendiagnostik vid sjukdom – och innan den bryter ut
2003) p.31-31(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Cytogenetic and molecular genetic evolution of Phi
2003) p.44-44(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Medicinsk genetik – en introduktion.
2003)(
- Book/Report › Book
-
Mark
Cytogenetic and Molecular Genetic Evolution of Philadelphia-Chromosome-Positive Chronic Myeloid Leukaemia
2003) p.44-61(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Cytogenetic and molecular genetic analyses of endometrial stromal sarcoma: nonrandom involvement of chromosome arms 6p and 7p and confirmation of JAZF1/JJAZ1 gene fusion in t(7;17)
(
- Contribution to journal › Article
- 2002
-
Mark
Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres.
(
- Contribution to journal › Article
-
Mark
Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.
(
- Contribution to journal › Article
-
Mark
Unaltered pancreatic islet blood perfusion in islet amyloid polypeptide-deficient mice
(
- Contribution to journal › Article
-
Mark
Delay between fusion pore opening and peptide release from large dense-core vesicles in neuroendocrine cells.
(
- Contribution to journal › Article
-
Mark
Frequent amplification of 8q24, 11q, 17q, and 20q-specific genes in pancreatic cancer
(
- Contribution to journal › Article
-
Mark
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group
(
- Contribution to journal › Article
-
Mark
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
(
- Contribution to journal › Article
-
Mark
Cytogenetic aberrations and their prognostic impact in chondrosarcoma
(
- Contribution to journal › Article
-
Mark
RT-PCR analysis of acute myeloid leukemia with t(8;16)(p11;p13): Identification of a novel MOZ/CBP transcript and absence of CBP/MOZ expression.
(
- Contribution to journal › Letter
-
Mark
Involvement and functional impairment of the CD34(+)CD38(-)Thy-1(+) hematopoietic stem cell pool in myelodysplastic syndromes with trisomy 8.
(
- 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
-
Mark
Cytogenetic and molecular genetic evolution of chronic myeloid leukemia.
(
- Contribution to journal › Scientific review
-
Mark
RNA splicing mediated by YB-1 is inhibited by TLS/CHOP in human myxoid liposarcoma cells
(
- Contribution to journal › Article
-
Mark
Expression of NUP98/TOP1, but not of TOP1/NUP98, in a treatment-related myelodysplastic syndrome with t(10;20;11)(q24;q11;p15).
(
- Contribution to journal › Article
-
Mark
Unique balanced chromosome abnormalities in treatment-related myelodysplastic syndromes and acute myeloid leukemia: Report from an international workshop
(
- Contribution to journal › Article
-
Mark
Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.
(
- Contribution to journal › Article
-
Mark
Cytogenetic features of multiple myeloma: impact of gender, age, disease phase, culture time, and cytokine stimulation
(
- Contribution to journal › Article
-
Mark
Acute myeloid leukemia with inv(16)(p13q22): Involvement of cervical lymph nodes and tonsils is common and may be a negative prognostic sign.
(
- Contribution to journal › Article
-
Mark
Detailed genomic mapping and expression analyses of 12p amplifications in pancreatic carcinomas reveal a 3.5-Mb target region for amplification.
(
- Contribution to journal › Article
-
Mark
Cyclin D1 amplification in chromosomal band 11q13 is associated with overrepresentation of 3q21-q29 in head and neck carcinomas.
(
- Contribution to journal › Article
-
Mark
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
(
- Contribution to journal › Article
-
Mark
Establishment and characterisation of a human clear cell sarcoma model in nude mice
(
- Contribution to journal › Article
-
Mark
Co-existence of SYT-SSX1 and SYT-SSX2 fusions in synovial sarcomas
(
- Contribution to journal › Article
-
Mark
Multivariate analysis of chromosomal imbalances in breast cancer delineates cytogenetic pathways and reveals complex relationships among imbalances.
(
- Contribution to journal › Article
-
Mark
Rapid identification of frequent MLL rearrangements in hematologic malignancies by multiplex RT-PCR in a single assay - Reply
(
- Contribution to journal › Letter
-
Mark
Dissecting karyotypic patterns in colorectal tumors: two distinct but overlapping pathways in the adenoma-carcinoma transition.
(
- Contribution to journal › Article
-
Mark
Pooled analysis of clinical and cytogenetic features in treatment-related and de novo adult acute myeloid leukemia and myelodysplastic syndromes based on a consecutive series of 761 patients analyzed 1976-1993 and on 5098 unselected cases reported in the literature 1974-2001.
(
- Contribution to journal › Article
-
Mark
Prognostic implications of BCL6 rearrangement in uniformly treated patients with diffuse large B-cell lymphoma--a Nordic Lymphoma Group study.
(
- Contribution to journal › Article
-
Mark
Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors.
(
- Contribution to journal › Article
-
Mark
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
(
- Contribution to journal › Article
-
Mark
Fusion of the FUS and ATF1 genes in a large, deep-seated angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
-
Mark
Cytogenetic abnormalities in a hemangiopericytoma of the spleen.
(
- Contribution to journal › Article
-
Mark
Tumour morphology--interplay between chromosome aberrations and founder cell differentiation.
(
- Contribution to journal › Scientific review
-
Mark
Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15.
(
- Contribution to journal › Article
-
Mark
Chromosomal translocations involving 11q13 contribute to cyclin D1 overexpression in squamous cell carcinoma of the head and neck
(
- Contribution to journal › Article
-
Mark
Coping with complexity. multivariate analysis of tumor karyotypes.
(
- Contribution to journal › Article
-
Mark
SYT-SSX is critical for cyclin D1 expression in synovial sarcoma cells: A gain of function of the t(X;18)(p11.2;q11.2) translocation
(
- Contribution to journal › Article
-
Mark
Chromosomal aberrations in benign and malignant Bilharzia-associated bladder lesions analyzed by comparative genomic hybridization.
(
- Contribution to journal › Article
-
Mark
Karyotypic heterogeneity and clonal evolution in squamous cell carcinomas of the head and neck.
(
- Contribution to journal › Article
-
Mark
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group.
(
- Contribution to journal › Article
-
Mark
Cytogenetic aberrations and heterogeneity of mutations in repeat-containing genes in a colon carcinoma from a patient with hereditary nonpolyposis colorectal cancer.
(
- Contribution to journal › Article
-
Mark
Proteoglycan production in disomic and trisomy 7-carrying human synovial cells.
(
- Contribution to journal › Article
-
Mark
Rapid identification of frequent MLL rearrangements in hematologic malignancies by multiplex RT-PCR in a single assay - Reply
(
- Contribution to journal › Letter
-
Mark
Alterations of the fragile histidine triad gene, FHIT, and its encoded products contribute to testicular germ cell tumorigenesis
(
- Contribution to journal › Article
-
Mark
Synovial chondromatosis
2002) p.246-246(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Congenital and inherited syndromes associated with bone and soft tissue tumours
2002) p.349-349(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone
- Book/Report › Anthology (editor)
-
Mark
Enchondromatosis: Ollier disease and Maffucci syndrome
2002) p.356-356(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Clonal chromosome abnormalities in premalignant lesions of the skin.
(
- Contribution to journal › Article
-
Mark
Chordoma
2002) p.316-316(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Solid tumor cytogenetics
2002) p.704-704(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2001
-
Mark
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors
(
- Contribution to journal › Article
-
Mark
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution
(
- Contribution to journal › Article
-
Mark
Issues in Human GenEthics
(
- Contribution to journal › Article
-
Mark
Cloning of the der(17)t(X;17)(p11;q25) alveolar soft part sarcoma identifies the ASPL-TFE3 gene fusion, a new molecular diagnostic marker
(
- Contribution to journal › Article
-
Mark
Abnormal nuclear shape in solid tumors reflects mitotic instability
(
- Contribution to journal › Article
-
Mark
Clinical impact of molecular and cytogenetic findings in synovial sarcoma
(
- Contribution to journal › Article
-
Mark
The absence of high-frequency QRS changes in the presence of standard electrocardiographic QRS changes of old myocardial infarction
(
- Contribution to journal › Article
-
Mark
Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH
(
- Contribution to journal › Article
-
Mark
Distinct cytologic features of spindle cell lipoma - A cytologic-histologic study with clinical, radiologic, electron microscopic, and cytogenetic correlations
(
- Contribution to journal › Article
-
Mark
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
(
- Contribution to journal › Article
-
Mark
Biallelic inactivation of TP53 rarely contributes to the development of malignant peripheral nerve sheath tumors
(
- Contribution to journal › Article
-
Mark
Proliferation of primitive myeloid progenitors can be reversibly induced by HOXA10
(
- Contribution to journal › Article
-
Mark
Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder
(
- Contribution to journal › Published meeting abstract
-
Mark
Smoking and acute myeloid leukemia: associations with morphology and karyotypic patterns and evaluation of dose-response relations
2001) In Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis 25(10). p.865-872(
- Contribution to journal › Article
-
Mark
Involvement and intrinsic deficiencies of hematopoietic stem cells in MDS patients with trisomy 8
(
- Contribution to journal › Article
-
Mark
Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)
(
- Contribution to journal › Article
-
Mark
Essential genetics education for non-genetics health professionals (EC Project GenEd)
(
- Contribution to journal › Article
-
Mark
Comparative genomic hybridization of postirradiation sarcomas
(
- Contribution to journal › Article
-
Mark
Characterization of chromosomal abnormalities in uroepithelial carcinomas by G-banding, spectral karyotyping and fish analysis
(
- Contribution to journal › Article
-
Mark
The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25
(
- Contribution to journal › Article
-
Mark
Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping
(
- Contribution to journal › Article
-
Mark
Trisomy 7 accumulates with age in solid tumors and non-neoplastic synovia
(
- Contribution to journal › Article
-
Mark
Fusion of the BCR and the fibroblast growth factor receptor-1 (FGFR1) genes as a result of t(8;22)(p11;q11) in a myeloproliferative disorder: the first fusion gene involving BCR but not ABL
(
- Contribution to journal › Article
-
Mark
No EWS/FLI1 fusion transcripts in giant-cell tumors of bone
(
- Contribution to journal › Article
-
Mark
Isodicentric 7p, idic(7)(q11.2), in acute myeloid
(
- Contribution to journal › Article
-
Mark
The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex
(
- Contribution to journal › Article
-
Mark
Identification of human candidate genes for male infertility by digital differential display
(
- Contribution to journal › Article
-
Mark
PLAG1 alterations in lipoblastoma: involvement in varied mesenchymal cell types and evidence for alternative oncogenic mechanisms
(
- Contribution to journal › Article
-
Mark
Limitations of chromosome classification by multicolor karyotyping
(
- Contribution to journal › Article
-
Mark
Paired multiplex reverse-transcriptase polymerase chain reaction (PMRT-PCR) analysis as a rapid and accurate diagnostic tool for the detection of MLL fusion genes in hematologic malignancies
(
- Contribution to journal › Article
-
Mark
Refined characterisation of chromosome aberrations in tumours by multicolour banding and electronic mapping resources
2001) In Methods in cell science: an official journal of the Society for In Vitro Biology 23(1-3). p.23-28(
- Contribution to journal › Article
-
Mark
Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer
(
- Contribution to journal › Article
-
Mark
Cloning of the der(17)t(X;17)(p11;q25) of alveolar soft part sarcoma identifies the ASPL-TFE3 gene fusion, a new molecular diagnostic marker
(
- Contribution to journal › Article
-
Mark
Analysis of the distribution and frequency of trisomy 7 in vivo in synovia from patients with osteoarthritis and pigmented villonodular synovitis
(
- Contribution to journal › Article
-
Mark
Are occupational, hobby, or lifestyle exposures associated with Philadelphia chromosome positive chronic myeloid leukaemia?
(
- Contribution to journal › Article
-
Mark
The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology
(
- Contribution to journal › Article
-
Mark
ETV6 rearrangements in patients with infantile fibrosarcomas and congenital mesoblastic nephromas by fluorescence in situ hybridization
(
- Contribution to journal › Article
-
Mark
Cytogenetic and fluorescence in situ hybridization characterization of chromosome 8 rearrangements in head and neck squamous cell carcinomas
(
- Contribution to journal › Article
-
Mark
Extensive cytogenetic heterogeneity in a benign retroperitoneal schwannoma
(
- Contribution to journal › Article
-
Mark
Altered expression of TGFB receptors and mitogenic effects of TGFB in pancreatic carcinomas
(
- Contribution to journal › Article
-
Mark
DNA copy number amplifications in sarcomas with homogeneously staining regions and double minutes
(
- Contribution to journal › Article
-
Mark
Calcium pyrophosphate dihydrate crystal deposition disease in the temporomandibular joint: Diagnostic difficulties and clonal chromosome aberrations in a case followed up for 5 years
(
- Contribution to journal › Article
-
Mark
Identification of cytogenetic subgroups and karyotypic pathways in transitional cell carcinoma
(
- Contribution to journal › Article
-
Mark
Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13)
(
- Contribution to journal › Article
-
Mark
The tumor-associated gene HMGIC is expressed in normal and osteoarthritis-affected synovia
(
- Contribution to journal › Article
-
Mark
Characterization of somatic mutations in nonneoplastic cells
2001)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Molecular studies of pancreatic cancer: Characterization of the transforming growth factor beta signaling pathway
2001)(
- Thesis › Doctoral thesis (compilation)
- 2000
-
Mark
Characterization of genomically amplified segments using PCR: optimizing relative-PCR for reliable and simple gene expression and gene copy analyses
(
- Contribution to journal › Article
-
Mark
Naturvetare och kulturforskare kan överbrygga ämnesgränser
(
- Contribution to journal › Article
-
Mark
Putting chromosome aberrations on the map
(
- Contribution to journal › Article
-
Mark
Granulocytic sarcomas in body cavities in childhood acute myeloid leukemias with 11q23/MLL rearrangements
(
- Contribution to journal › Article
-
Mark
RT-PCR analysis of the MOZ-CBP and CBP-MOZ chimeric transcripts in acute myeloid leukemias with t(8;16)(p11;p13)
(
- Contribution to journal › Article
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Mark
BRCA1 and BRCA2 mutations in ovarian cancer : Covariation with specific cytogenetic features
(
- Contribution to journal › Article
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Mark
Smoking and myelodysplastic syndromes
(
- Contribution to journal › Article
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Mark
Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study
(
- Contribution to journal › Article
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Mark
Locus-specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasia
(
- Contribution to journal › Article
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Mark
Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias
(
- Contribution to journal › Article
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Mark
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
(
- Contribution to journal › Article
-
Mark
Survival time in a population-based consecutive series of adult acute myeloid leukemia--the prognostic impact of karyotype during the time period 1976-1993
(
- Contribution to journal › Article
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Mark
Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p
(
- Contribution to journal › Article
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Mark
Cytogenetic heterogeneity and clonal evolution in synchronous bilateral breast carcinomas and their lymph node metastases from a male patient without any detectable BRCA2 germline mutation
(
- Contribution to journal › Article
-
Mark
Chromosomal Instability and Genomic Amplification in Bone and Soft Tissue Tumours
2000)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer
(
- Contribution to journal › Article
-
Mark
High-Frequency ECG in Ischemic Heart Disease
2000)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Fast isolation of proteins from bioreactors using affinity chromatography techniques
2000)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Spatial, individual and temporal variation of the high frequency QRS amplitudes in the 12 standard electrocardiographic leads
(
- Contribution to journal › Article
-
Mark
Changes in high-frequency QRS components are more sensitive than ST segment deviation for detecting acute coronary artery occlusion
(
- Contribution to journal › Article
-
Mark
Lentivirus vector gene expression during ES cell-derived hematopoietic development in vitro
(
- Contribution to journal › Article
-
Mark
Identification and Characterization of Novel Candidate Oncogenes
2000)(
- Thesis › Doctoral thesis (compilation)
- 1999
-
Mark
Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations
(
- Contribution to journal › Article
-
Mark
A single-center population-based consecutive series of 1500 cytogenetically investigated adult hematological malignancies: karyotypic features in relation to morphology, age and gender
(
- Contribution to journal › Article
-
Mark
Cytogenetic aberrations in Ewing sarcoma: are secondary changes associated with clinical outcome?
(
- Contribution to journal › Article
-
Mark
Prognostic implications of cytogenetic aberrations in diffuse large B-cell lymphomas
(
- Contribution to journal › Article
-
Mark
Cytogenetic polyclonality in hematologic malignancies
(
- Contribution to journal › Article
-
Mark
Chromosomal aberrations in breast cancer: a comparison between cytogenetics and comparative genomic hybridization
(
- Contribution to journal › Article
-
Mark
hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden
(
- Contribution to journal › Article
-
Mark
Hibernomas are characterized by homozygous deletions in the multiple endocrine neoplasia type I region. Metaphase fluorescence in situ hybridization reveals complex rearrangements not detected by conventional cytogenetics
(
- Contribution to journal › Article
-
Mark
Unique cytological features and chromosome aberrations in chondroid lipoma: a case report based on fine-needle aspiration cytology, histopathology, electron microscopy, chromosome banding, and molecular cytogenetics
(
- Contribution to journal › Article
-
Mark
Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers
(
- Contribution to journal › Article
-
Mark
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells
(
- Contribution to journal › Article
-
Mark
Variable stability of chromosomes containing amplified alpha-satellite sequences in human mesenchymal tumours
(
- Contribution to journal › Article
-
Mark
CAG repeat length in the androgen receptor gene is related to age at diagnosis of prostate cancer and response to endocrine therapy, but not to prostate cancer risk
(
- Contribution to journal › Article
-
Mark
Familial and hereditary prostate cancer in southern Sweden. A population-based case-control study
(
- Contribution to journal › Article
-
Mark
Rearrangement of the neoplasia-associated gene HMGIC in synovia from patients with osteoarthritis
(
- Contribution to journal › Article
-
Mark
Cytogenetic analyses of secondary liver tumors reveal significant differences in genomic imbalances between primary and metastatic colon carcinomas
(
- Contribution to journal › Article
-
Mark
Nonrandom chromosomal aberrations and cytogenetic heterogeneity in gallbladder carcinomas
(
- Contribution to journal › Article
-
Mark
Cytogenetic studies of primary and metastatic breast cancer
1999)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Abnormal cell cycle regulation in malignancy
(
- Contribution to journal › Scientific review
- 1998
-
Mark
Complex karyotypes in flow cytometrically DNA-diploid squamous cell carcinomas of the head and neck
(
- Contribution to journal › Article
-
Mark
Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization
(
- Contribution to journal › Article
-
Mark
Amplification of 12q13 and 12q15 sequences in a sclerosing epithelioid fibrosarcoma
(
- Contribution to journal › Article
-
Mark
A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences
(
- Contribution to journal › Article
-
Mark
ETV6/ABL fusion is rare in Ph-negative chronic myeloid disorders
(
- Contribution to journal › Article
-
Mark
A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences
(
- Contribution to journal › Article
-
Mark
Clinical course of early onset prostate cancer with special reference to family history as a prognostic factor
(
- Contribution to journal › Article
-
Mark
Forskningsframsteg om hereditär prostatacancer. Riskfamiljer bör kartläggas och erbjudas screening
(
- Contribution to journal › Article
-
Mark
Cytogenetic studies of benign breast lesions
1998)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Frequent rearrangements of chromosomes 1, 7, and 8 in primary liver cancer
(
- Contribution to journal › Article
- 1997
-
Mark
Poor survival in t(8;21) (q22;q22)-associated acute myeloid leukaemia with leukocytosis
(
- Contribution to journal › Article
-
Mark
Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer
(
- Contribution to journal › Article
-
Mark
BCR/ABL-negative chronic myeloid leukemia with ETV6/ABL fusion
(
- Contribution to journal › Article
-
Mark
Cytogenetic abnormalities and clonal evolution in an adult hepatoblastoma
(
- Contribution to journal › Article
-
Mark
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
(
- Contribution to journal › Article
-
Mark
The risk of malignant tumours in first-degree relatives of men with early onset prostate cancer : a population-based cohort study
(
- Contribution to journal › Article
-
Mark
Sons of men with prostate cancer : their attitudes regarding possible inheritance of prostate cancer, screening, and genetic testing
(
- Contribution to journal › Article
-
Mark
Clonal chromosome aberrations are present in vivo in synovia and osteophytes from patients with osteoarthritis
(
- Contribution to journal › Article
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Mark
Monosomy 22 in a case of biliary adenofibroma
(
- Contribution to journal › Article
-
Mark
Hypereosinophilic syndrome in a child mosaic for a congenital triplication of the short arm of chromosome 8
(
- Contribution to journal › Article
- 1996
-
Mark
Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families
(
- Contribution to journal › Article
-
Mark
t(3;21)(q26;q22) with AML1 rearrangement in a de novo childhood acute monoblastic leukaemia
(
- Contribution to journal › Article
-
Mark
Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS
(
- Contribution to journal › Article
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Mark
Abberant cytogenetic evolution pattern of Philadelphia-positive chronic myeloid leukemia treated with interferon-alpha
(
- Contribution to journal › Article
-
Mark
Emergence of novel transient clonal chromosomal bone marrow changes in remission of acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
Correlation between karyotypic pattern and clincopathologic features in 125 breast cancer cases
(
- Contribution to journal › Article
-
Mark
Molecular Genetic Studies of Ph-positive Leukemias and the BCR and ABL Genes
1996)(
- Thesis › Doctoral thesis (compilation)
- 1995
-
Mark
Standpoint on imprinting of BCR and ABL
(
- Contribution to journal › Article
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Mark
Regional localization and developmental expression of the BCR gene in rodent brain
(
- Contribution to journal › Article
- 1994
-
Mark
Molecular analysis of simple variant translocations in acute promyelocytic leukemia
(
- Contribution to journal › Article
-
Mark
Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22)
(
- Contribution to journal › Article
-
Mark
No evidence for genomic imprinting of the human BCR gene
(
- Contribution to journal › Article
- 1993
-
Mark
Cytogenetic findings in 33 osteosarcomas
(
- Contribution to journal › Article
-
Mark
Comparative cytogenetic and DNA flow cytometric analysis of 150 bone and soft-tissue tumors
(
- Contribution to journal › Article