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- 2014
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Mark
Special section editorial.
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- Contribution to journal › Debate/Note/Editorial
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Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
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- Contribution to journal › Article
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Mark
Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer.
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- Contribution to journal › Article
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Mark
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
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- Contribution to journal › Article
- 2013
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Mark
rs2072135, a low-penetrance variant for chronic lymphocytic leukaemia?
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- Contribution to journal › Article
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Mark
Genome-wide association study on differentiated thyroid cancer.
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- Contribution to journal › Article
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Mark
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma
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- Contribution to journal › Article
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Mark
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype
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- Contribution to journal › Article
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Mark
The CCND1 c.870G > A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
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- Contribution to journal › Article
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Mark
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
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- Contribution to journal › Article