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- 2004
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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
- 2003
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Mark
Pancreatic carcinoma cell lines with SMAD4 inactivation show distinct expression responses to TGFB1.
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- Contribution to journal › Article
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Mark
A pooled analysis of karyotypic patterns, breakpoints and imbalances in 783 cytogenetically abnormal multiple myelomas reveals frequently involved chromosome segments as well as significant age- and sex-related differences.
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- Contribution to journal › Article
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Mark
A Novel Gene, MSI2, Encoding a Putative RNA-binding Protein Is Recurrently Rearranged at Disease Progression of Chronic Myeloid Leukemia and Forms a Fusion Gene with HOXA9 as a Result of the Cryptic t(7;17)(p15;q23).
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- Contribution to journal › Article
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Mark
Clinical and genetic studies of ETV6/ABL1-positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylate.
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- Contribution to journal › Article
- 2002
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Mark
Detailed genomic mapping and expression analyses of 12p amplifications in pancreatic carcinomas reveal a 3.5-Mb target region for amplification.
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- Contribution to journal › Article
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Mark
Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.
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- Contribution to journal › Article
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Mark
Cytogenetic features of multiple myeloma: impact of gender, age, disease phase, culture time, and cytokine stimulation
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- Contribution to journal › Article
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Mark
Acute myeloid leukemia with inv(16)(p13q22): Involvement of cervical lymph nodes and tonsils is common and may be a negative prognostic sign.
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- Contribution to journal › Article
- 2001
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Mark
Extensive cytogenetic heterogeneity in a benign retroperitoneal schwannoma
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- Contribution to journal › Article