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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
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Mark
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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Mark
Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.
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- Contribution to journal › Article
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Mark
Wilms tumors develop through two distinct karyotypic pathways.
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- Contribution to journal › Article
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Mark
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
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- Contribution to journal › Article
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Mark
Statistical dissection of cytogenetic patterns in lung cancer reveals multiple modes of karyotypic evolution independent of histological classification.
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- Contribution to journal › Article
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Mark
Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines.
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- Contribution to journal › Article
- 2003
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Mark
Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors
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- Contribution to journal › Article
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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