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- 2013
-
Mark
The CCND1 c.870G > A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
(
- Contribution to journal › Article
-
Mark
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
(
- Contribution to journal › Article
- 2011
-
Mark
Consensus Pathways Implicated in Prognosis of Colorectal Cancer Identified Through Systematic Enrichment Analysis of Gene Expression Profiling Studies
(
- Contribution to journal › Article
-
Mark
Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome
(
- Contribution to journal › Article
- 2010
-
Mark
Breast and prostate cancer: familial associations
(
- Contribution to journal › Letter
-
Mark
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients
(
- Contribution to journal › Article
-
Mark
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility
(
- Contribution to journal › Article
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