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- 2005
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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
- 2004
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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
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
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
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
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
Approximate geodesic distances reveal biologically relevant structures in microarray data
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- Contribution to journal › Article
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Mark
Vascular endothelial growth factor gene polymorphisms and pre-eclampsia
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- Contribution to journal › Article