Division of Clinical Genetics
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- 2004
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Mark
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
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- Contribution to journal › Article
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Mark
Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas.
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- Contribution to journal › Article
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Mark
Cytogenetic and molecular genetic characterization of immortalized human ovarian surface epithelial cell lines: consistent loss of chromosome 13 and amplification of chromosome 20
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- Contribution to journal › Article
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Mark
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia
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- Contribution to journal › Scientific review
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Mark
Sudanesiska cytogenetiker - vision om en ny form av bistånd
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- Contribution to journal › Article
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Mark
Mitotic instability associated with late genomic changes in bone and soft tissue tumours.
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- Contribution to journal › Article
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Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.
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- Contribution to journal › Article
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Wilms tumors develop through two distinct karyotypic pathways.
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- Contribution to journal › Article
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Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
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- Contribution to journal › Article
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Genome characteristics of primary carcinomas, local recurrences, carcinomatoses, and liver metastases from colorectal cancer patients
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- Contribution to journal › Article
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Mark
Statistical dissection of cytogenetic patterns in lung cancer reveals multiple modes of karyotypic evolution independent of histological classification.
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- 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
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- Contribution to journal › Article
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Establishment and phenotypic characterization of human U937 cells with inducible P210 BCR/ABL expression reveals upregulation of CEACAM1 (CD66a).
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- Contribution to journal › Article
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Mark
Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.
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- Contribution to journal › Article
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Mark
Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma
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- Contribution to journal › Article
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Mark
External quality assessment for mutation detection in the BRCA1 and BRCA2 genes: EMQN's experience of 3 years
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- Contribution to journal › Article
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Mark
Comparison of signal quality between EASI and Mason-Likar 12-lead electrocardiograms during physical activity.
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- Contribution to journal › Article
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Mark
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer
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- Contribution to journal › Article
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Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12).
(
- Contribution to journal › Article
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Mark
Genetic analyses of multiple myeloma and related plasma cell dyscrasias
2004)(
- Thesis › Doctoral thesis (compilation)
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Mark
Genetisk rådgivning och fosterdiagnostik.
2004) p.56-56(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Molecular Characterization of Genomic Amplifications in Pancreatic Cancer
2004)(
- Thesis › Doctoral thesis (compilation)
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Mark
Studies on Molecular Genetics of B cell Development
2004)(
- Thesis › Doctoral thesis (compilation)
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Mark
The need for oncogenetic counselling - Ten years' experience of a regional oncogenetic clinic
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- Contribution to journal › Article
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Mark
Characterization of Genetic Abnormalities at Disease Progression of Chronic Myeloid Leukemia
2004)(
- Thesis › Doctoral thesis (compilation)
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Mark
Genetic characterization of bone and soft tissue tumors
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- Contribution to journal › Article
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Mark
Expression of DOL54 is not restricted to myxoid liposarcomas with the FUS-DDIT3 chimera but is found in various sarcomas.1
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- Contribution to journal › Article
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Mark
Cytogenetic and fluorescence in situ hybridization characterization of clonal chromosomal aberrations and CCND1 amplification in esophageal carcinomas
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- Contribution to journal › Article
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Mark
Regulation of genetic testing in clinical practice
(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2003
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Mark
Prevalence of hemochromatosis gene (HFE) mutations in Greece
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- Contribution to journal › Article
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Mark
Population genetic screening programmes: technical, social, and ethical issues.
(
- 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
The relative accuracies of ECG precordial lead waveforms derived from EASI leads and those acquired from paramedic applied standard leads
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- Contribution to journal › Article
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Mark
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia.
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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
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- 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
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma
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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.
(
- 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
Pancreatic carcinoma cell lines with SMAD4 inactivation show distinct expression responses to TGFB1.
(
- 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
(
- Contribution to journal › Article
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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.
(
- 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
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
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
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
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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A novel fusion gene, SS18L1/SSX1, in synovial sarcoma
(
- Contribution to journal › Article
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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
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
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
Characterization of a novel breast carcinoma xenograft and cell line derived from a BRCA1 germ-line mutation carrier
(
- 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
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
Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas
(
- 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
Power law distribution of chromosome aberrations in cancer.
(
- 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
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
Cytogenetic and molecular genetic evolution of Phi
2003) p.44-44(
- 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
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
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
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
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
Chromosomal abnormalities in inflammatory pseudotumor of the urinary bladder
(
- 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
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
Chromosome instability in cancer: how, when, and why?
(
- Contribution to journal › Scientific review
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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
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
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
- 2002
-
Mark
Cytogenetic aberrations and their prognostic impact in chondrosarcoma
(
- Contribution to journal › Article
-
Mark
Cytogenetic and molecular genetic evolution of chronic myeloid leukemia.
(
- Contribution to journal › Scientific review
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Mark
Delay between fusion pore opening and peptide release from large dense-core vesicles in neuroendocrine cells.
(
- Contribution to journal › Article
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Mark
Unaltered pancreatic islet blood perfusion in islet amyloid polypeptide-deficient mice
(
- Contribution to journal › Article
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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
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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
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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
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
Frequent amplification of 8q24, 11q, 17q, and 20q-specific genes in pancreatic cancer
(
- Contribution to journal › Article
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Mark
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
(
- Contribution to journal › Article
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Mark
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.
(
- Contribution to journal › Article
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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
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
RNA splicing mediated by YB-1 is inhibited by TLS/CHOP in human myxoid liposarcoma cells
(
- 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
Establishment and characterisation of a human clear cell sarcoma model in nude mice
(
- Contribution to journal › Article
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Mark
Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres.
(
- Contribution to journal › Article
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Mark
Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.
(
- Contribution to journal › Article
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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
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Mark
Co-existence of SYT-SSX1 and SYT-SSX2 fusions in synovial sarcomas
(
- Contribution to journal › Article
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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