Johan Staaf
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- 2008
-
Mark
Array-CGH identifies cyclin D1 and UBCH10 amplicons in anaplastic thyroid carcinoma.
- Contribution to journal › Article
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Mark
Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios.
- Contribution to journal › Article
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Mark
Recurrent gross mutations of the PTEN tumor suppressor gene in breast cancers with deficient DSB repair
- Contribution to journal › Article
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Mark
Effect of polyamine deficiency on proteins involved in Okazaki fragment maturation.
- Contribution to journal › Article
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Mark
Array-CGH reveals hidden gene dose changes in children with acute lymphoblastic leukaemia and a normal or failed karyotype by G-banding
- Contribution to journal › Article
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Mark
Genomic alterations in coleorectal cencer in relationship to stage and survival assesed by tiling BAC array CGH
- Contribution to journal › Published meeting abstract
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Mark
Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia-A comparative study of four differently designed, high resolution microarray platforms.
- Contribution to journal › Article
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Mark
Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms
- Contribution to journal › Article
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Mark
Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays
- Contribution to journal › Article
- 2007
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Mark
Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities
- Contribution to journal › Article
