Division of Clinical Genetics
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- 2015
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Mark
The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article
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A certified plasmid reference material for the standardisation of BCR-ABL1 mRNA quantification by real time quantitative PCR.
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- Contribution to journal › Article
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FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
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- Contribution to journal › Article
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Mark
Methylated RASSF1A in malignant peripheral nerve sheath tumors identifies neurofibromatosis type 1 patients with inferior prognosis.
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- Contribution to journal › Article
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Mark
The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013.
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- Contribution to journal › Article
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Mark
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.
2015) In European Journal of Human Genetics(
- Contribution to journal › Article
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Mark
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
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- Contribution to journal › Article
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Mark
Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1.
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- Contribution to journal › Article
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The DEK oncoprotein and its emerging roles in gene regulation.
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- Contribution to journal › Scientific review
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Recurrent PRDM10 Gene Fusions in Undifferentiated Pleomorphic Sarcoma.
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- Contribution to journal › Article