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- 2011
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Mark
Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?
(
- Contribution to journal › Letter
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Mark
Identification of a Novel, Recurrent HEY1-NCOA2 Fusion in Mesenchymal Chondrosarcoma Based on a Genome-Wide Screen of Exon-Level Expression Data
2011) Annual Meeting on the United States and Canadian-Academy-of-Pathology, 2011 In Laboratory Investigation 91. p.23-23(
- Contribution to journal › Published meeting abstract
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Mark
Comparison of Six Statistics of Genetic Association Regarding Their Ability to Discriminate between Causal Variants and Genetically Linked Markers
(
- Contribution to journal › Article
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Mark
Blood Pressure Loci Identified with a Gene-Centric Array
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- Contribution to journal › Article
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Mark
High-resolution genomic profiling of an adult Wilms' tumor: evidence for a pathogenesis distinct from corresponding pediatric tumors.
(
- Contribution to journal › Article
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Mark
Mutation (variation) databases and registries: a rationale for coordination of efforts.
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- Contribution to journal › Letter
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Mark
PROlocalizer: integrated web service for protein subcellular localization prediction.
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- Contribution to journal › Article
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Mark
Gene expression and single nucleotide polymorphism array analyses of spindle cell lipomas and conventional lipomas with 13q14 deletion.
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- Contribution to journal › Article
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Mark
High-resolution genomic screening in mantle cell lymphoma--specific changes correlate with genomic complexity, the proliferation signature and survival.
(
- Contribution to journal › Article
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Mark
Alternative lengthening of telomeres-An enhanced chromosomal instability in aggressive non-MYCN amplified and telomere elongated neuroblastomas.
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- Contribution to journal › Article