Division of Clinical Genetics
1001 – 1010 of 1274
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- 2004
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Mark
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparation.
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- Contribution to journal › Article
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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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Abstracts from the Ninth Annual Meeting of the Society for Neuro-Oncology
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- Contribution to journal › Article
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Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies.
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- Contribution to journal › Article
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Mark
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients.
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- Contribution to journal › Article
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One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
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- Contribution to journal › Article
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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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Cytogenetic and molecular genetic characterization of immortalized human ovarian surface epithelial cell lines: consistent loss of chromosome 13 and amplification of chromosome 20
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- Contribution to journal › Article
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Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia
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- Contribution to journal › Scientific review
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Reduced high-frequency QRS components in patients with ischemic heart disease compared to normal subjects
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- Contribution to journal › Article