Division of Clinical Genetics
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- 2014
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Mark
Prognostic Implications of Mutations in NOTCH1 and FBXW7 in Childhood T-ALL Treated According to the NOPHO ALL-1992 and ALL-2000 Protocols
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- Contribution to journal › Article
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Mark
Fusions involving protein kinase C and membrane-associated proteins in benign fibrous histiocytoma.
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- Contribution to journal › Article
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Mark
A novel SERPINE1-FOSB fusion gene results in transcriptional up-regulation of FOSB in pseudomyogenic haemangioendothelioma.
(
- Contribution to journal › Article
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Mark
Evolving techniques for gene fusion detection in soft tissue tumours.
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- Contribution to journal › Scientific review
- 2013
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Mark
Functional Modeling of Genes Upregulated in Chronic Myeloid Leukemia
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- Thesis › Doctoral thesis (compilation)
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Mark
Intratumour diversity of chromosome copy numbers in neuroblastoma mediated by on-going chromosome loss from a polyploid state.
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- Contribution to journal › Article
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Mark
Whole-genome-amplified DNA as a source for mutational analysis underestimates the frequency of mutations in pediatric acute myeloid leukemia
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- Contribution to journal › Letter
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Mark
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
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- Contribution to journal › Article
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Mark
Loss of chromosomes is the primary event in near-haploid and low hypodiploid acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
Assessment of Fusion Gene Status in Sarcomas Using a Custom Made Fusion Gene Microarray
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- Contribution to journal › Article