Division of Clinical Genetics
1001 – 1010 of 1270
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- 2004
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Mark
Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation.
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- Contribution to journal › Article
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Mark
An excess of chromosome 1 breakpoints in male infertility.
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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
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
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
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
- 2003
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Mark
Consequences of eliminating adenosine A(1) receptors in mice
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- 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.
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- Contribution to journal › Article