Division of Clinical Genetics
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- 2004
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Mark
Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation.
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- Contribution to journal › Article
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Mark
An excess of chromosome 1 breakpoints in male infertility.
(
- Contribution to journal › Article
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Mark
Autologous del(20q)-positive erythroid progenitor cells, re-emerging after DLI treatment of an MDS patient relapsing after allo-SCT, can provide a normal peripheral red blood cell count.
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- Contribution to journal › Article
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Mark
Identification of genes differentially regulated by the P210 BCR/ABL1 fusion oncogene using cDNA microarrays.
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- Contribution to journal › Article
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Mark
Molecular cytogenetic characterization of recurrent translocation breakpoints in bizarre parosteal osteochondromatous proliferation (Nora's lesion).
(
- Contribution to journal › Article
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Mark
Activation of the GLI Oncogene through Fusion with the beta-Actin Gene (ACTB) in a Group of Distinctive Pericytic Neoplasms: Pericytoma with t(7;12).
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- Contribution to journal › Article
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Mark
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1
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- Contribution to journal › Article
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Mark
The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma.
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- Contribution to journal › Article
- 2003
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Mark
Consequences of eliminating adenosine A(1) receptors in mice
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
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Mark
Provision of genetic service in Europe: current practices and issues.
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- Contribution to journal › Article
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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.
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- Contribution to journal › Article
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Mark
Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors
(
- Contribution to journal › Article
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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
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Mark
Reduced proliferative capacity of hematopoietic stem cells deficient in hoxb3 and hoxb4.
(
- Contribution to journal › Article
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Mark
Topoisomerase-II alpha is upregulated in malignant peripheral nerve sheath tumors and associated with clinical outcome
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- Contribution to journal › Article
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Mark
Characterization of a novel breast carcinoma xenograft and cell line derived from a BRCA1 germ-line mutation carrier
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- Contribution to journal › Article
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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
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Mark
Pancreatic carcinoma cell lines with SMAD4 inactivation show distinct expression responses to TGFB1.
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- Contribution to journal › Article
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Mark
Vitamin d receptor is expressed in pancreatic cancer cells and a vitamin d(3) analogue decreases cell number.
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- Contribution to journal › Article
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Mark
Genetic profiling of colorectal cancer liver metastases by combined comparative genomic hybridization and G-banding analysis
(
- Contribution to journal › Article
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Mark
Cytogenetic and morphologic subgroups of myelodysplastic syndromes in relation to occupational and hobby exposures.
(
- Contribution to journal › Article
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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
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Mark
Data storage and DNA banking for biomedical research: technical, social and ethical issues.
(
- Contribution to journal › Article
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Mark
Fusion, disruption, and expression of HMGA2 in bone and soft tissue chondromas
(
- Contribution to journal › Article
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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
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Mark
Ett etiskt dilemma: Farmakogenetiskt test kan ge oönskad information [An ethical dilemma: pharmacogenetic tests can yield unwanted information]
(
- Contribution to journal › Article
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Mark
Power law distribution of chromosome aberrations in cancer.
(
- Contribution to journal › Article
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Mark
Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas
(
- Contribution to journal › Article
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Mark
Chromosomal abnormalities in inflammatory pseudotumor of the urinary bladder
(
- Contribution to journal › Article
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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
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Mark
Chromosome instability in cancer: how, when, and why?
(
- Contribution to journal › Scientific review
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Mark
Lundensisk allvarshumor
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
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Mark
Ovarian Carcinoma Develops through Multiple Modes of Chromosomal Evolution.
(
- Contribution to journal › Article
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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
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Mark
Cytogenetic findings and clinical course in a consecutive series of Wilms tumors
(
- Contribution to journal › Article
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Mark
Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia
(
- Contribution to journal › Article
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Mark
MYC is not overexpressed in a case of chronic myelomonocytic leukemia with MYC-containing double minutes
(
- Contribution to journal › Letter
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Mark
Extraskeletal myxoid chondrosarcoma with neuroendocrine differentiation: a case report with fine-needle aspiration biopsy, histopathology, electron microscopy, and cytogenetics.
(
- Contribution to journal › Article
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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
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Mark
Statens medicinsk-etiska råd. Genetisk screening - om hälsa och ärftlig sjukdomsrisk. Etiska vägmärken 11. (rec)
(
- Contribution to journal › Article
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Mark
Cytogenetic and molecular genetic evolution of Phi
2003) p.44-44(
- Chapter in Book/Report/Conference proceeding › Book chapter
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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
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Mark
Medicinsk genetik – en introduktion.
2003)(
- Book/Report › Book
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Mark
Gendiagnostik vid sjukdom – och innan den bryter ut
2003) p.31-31(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Clinical and genetic studies of ETV6/ABL1-positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylate.
(
- Contribution to journal › Article
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Mark
Genetic information and testing insurance and employment: technical, social, and ethical issues.
(
- Contribution to journal › Article
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Mark
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma
(
- Contribution to journal › Article
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Mark
Prevalence of hemochromatosis gene (HFE) mutations in Greece
(
- Contribution to journal › Article
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Mark
Provision of genetic services in Europe: current practices and issues
(
- Contribution to journal › Article
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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
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Mark
A novel fusion gene, SS18L1/SSX1, in synovial sarcoma
(
- Contribution to journal › Article
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Mark
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1
(
- Contribution to journal › Published meeting abstract
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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
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Mark
Population genetic screening programmes: technical, social, and ethical issues.
(
- Contribution to journal › Article
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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
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Mark
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
- 2002
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Mark
Establishment and characterisation of a human clear cell sarcoma model in nude mice
(
- Contribution to journal › Article
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Mark
Cyclin D1 amplification in chromosomal band 11q13 is associated with overrepresentation of 3q21-q29 in head and neck carcinomas.
(
- Contribution to journal › Article
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Mark
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
(
- Contribution to journal › Article
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Mark
RNA splicing mediated by YB-1 is inhibited by TLS/CHOP in human myxoid liposarcoma cells
(
- 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
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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
Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.
(
- Contribution to journal › Article
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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
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Mark
Cytogenetic features of multiple myeloma: impact of gender, age, disease phase, culture time, and cytokine stimulation
(
- Contribution to journal › Article
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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
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Mark
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
(
- Contribution to journal › Article
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Mark
Fusion of the FUS and ATF1 genes in a large, deep-seated angiomatoid fibrous histiocytoma
(
- Contribution to journal › Article
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Mark
Rapid identification of frequent MLL rearrangements in hematologic malignancies by multiplex RT-PCR in a single assay - Reply
(
- Contribution to journal › Letter
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Mark
Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors.
(
- Contribution to journal › Article
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Mark
Multivariate analysis of chromosomal imbalances in breast cancer delineates cytogenetic pathways and reveals complex relationships among imbalances.
(
- Contribution to journal › Article
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Mark
Cytogenetic abnormalities in a hemangiopericytoma of the spleen.
(
- Contribution to journal › Article
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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
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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
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group.
(
- Contribution to journal › Article
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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
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
Karyotypic heterogeneity and clonal evolution in squamous cell carcinomas of the head and neck.
(
- Contribution to journal › Article
-
Mark
Chromosomal aberrations in benign and malignant Bilharzia-associated bladder lesions analyzed by comparative genomic hybridization.
(
- Contribution to journal › Article
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Mark
Clonal chromosome abnormalities in premalignant lesions of the skin.
(
- Contribution to journal › Article
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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
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Mark
Coping with complexity. multivariate analysis of tumor karyotypes.
(
- Contribution to journal › Article
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Mark
Alterations of the fragile histidine triad gene, FHIT, and its encoded products contribute to testicular germ cell tumorigenesis
(
- 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
Tumour morphology--interplay between chromosome aberrations and founder cell differentiation.
(
- Contribution to journal › Scientific review
-
Mark
Dissecting karyotypic patterns in colorectal tumors: two distinct but overlapping pathways in the adenoma-carcinoma transition.
(
- Contribution to journal › Article
-
Mark
Solid tumor cytogenetics
2002) p.704-704(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Synovial chondromatosis
2002) p.246-246(
- 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
Chordoma
2002) p.316-316(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Enchondromatosis: Ollier disease and Maffucci syndrome
2002) p.356-356(
- 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
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
(
- 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
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
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
Co-existence of SYT-SSX1 and SYT-SSX2 fusions in synovial sarcomas
(
- Contribution to journal › Article
-
Mark
Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres.
(
- Contribution to journal › Article