Division of Clinical Genetics
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- 2004
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Mark
Reduced high-frequency QRS components in patients with ischemic heart disease compared to normal subjects
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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
MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23).
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- Contribution to journal › Article
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Mark
Wilms tumors develop through two distinct karyotypic pathways.
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- Contribution to journal › Article
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Mark
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
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
Regulation of genetic testing in clinical practice
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- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12).
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- Contribution to journal › Article
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Mark
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
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- Contribution to journal › Article
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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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Mark
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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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
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
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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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
(
- 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
Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma
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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
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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Mark
A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.
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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
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.
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- Contribution to journal › Article
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Mark
Provision of genetic services in Europe: current practices and issues
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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
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
Provision of genetic service in Europe: current practices and issues.
(
- 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
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.
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- 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
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
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
Reduced proliferative capacity of hematopoietic stem cells deficient in hoxb3 and hoxb4.
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- 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
Cytogenetic and morphologic subgroups of myelodysplastic syndromes in relation to occupational and hobby exposures.
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- 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).
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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 › Published meeting abstract
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Mark
A novel fusion gene, SS18L1/SSX1, in synovial sarcoma
(
- 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?
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- Contribution to journal › Letter
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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