Division of Clinical Genetics
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- 2006
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Mark
Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration.
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- Contribution to journal › Article
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Mark
Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor.
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- Contribution to journal › Article
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Mark
Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays.
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- Contribution to journal › Article
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Mark
Meta- and synchronous urothelial carcinomas with divergent genomic profiles show highly similar gene-expression profiles
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- Contribution to journal › Published meeting abstract
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Mark
t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene
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- Contribution to journal › Letter
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Mark
Molecular and functional studies of the BCR/ABL1 fusion gene
2006)(
- Thesis › Doctoral thesis (compilation)
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Mark
Cytogenetic abnormalities in 106 oral squamous cell carcinomas
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- Contribution to journal › Article
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Mark
A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42
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- Contribution to journal › Article
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Mark
Antithymocyte globulin and cyclosporine A as combination therapy for low-risk non-sideroblastic myelodysplastic syndromes
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- Contribution to journal › Article