Division of Clinical Genetics
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- 2005
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Mark
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations
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- Contribution to journal › Article
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Mark
Nya rön om fragil X-syndromet komplicerar genetisk vägledning. Sjukdomsgenen orsakar fler symtom än vad som tidigare varit känt
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- Contribution to journal › Article
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Mark
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma.
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- Contribution to journal › Article
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Mark
Distinct patterns of hematopoietic stem cell involvement in acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12
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- Contribution to journal › Article
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Mark
Ny kunskap om arv och ärftlighet ger nya aspekter på hjärtsjukdom
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- Contribution to journal › Article
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Mark
Connecting mitotic instability and chromosome aberrations in cancer-can telomeres bridge the gap?
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- Contribution to journal › Scientific review
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Mark
Gene Expression Studies of Hematologic Malignacies
2005)(
- Thesis › Doctoral thesis (compilation)
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Mark
Euploidy in somatic cells from R6/2 transgenic Huntington's disease mice
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- Contribution to journal › Article
- 2004
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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
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).
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- 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
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
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Mark
The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.
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- Contribution to journal › Article
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Mark
Hoxb4-deficient mice undergo normal hematopoietic development but exhibit a mild proliferation defect in hematopoietic stem cells
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- Contribution to journal › Article
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Mark
MDS/AML-associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: Evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q).
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- Contribution to journal › Article
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Mark
Pearson correlation analysis of micro-array data allows for the identification of genetic targets for early B-cell factor.
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- Contribution to journal › Article
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Mark
Amylin inhibits bone resorption while the calcitonin receptor controls bone formation in vivo
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- Contribution to journal › Article