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- 2022
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Mark
Methylation and copy number profiling : emerging tools to differentiate osteoblastoma from malignant mimics?
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- Contribution to journal › Article
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Mark
Epigenetics of type 2 diabetes mellitus and weight change — a tool for precision medicine?
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- Contribution to journal › Scientific review
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Mark
Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis : How to Correctly Identify MODY8 Cases
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- Contribution to journal › Article
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Mark
Novel or not? Reference alleles, genes, and genomes to unmask the true nature of the ABO*AW.10 allele associated with weak A phenotype
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- Contribution to journal › Debate/Note/Editorial
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Mark
hnRNP G/RBMX enhances HPV16 E2 mRNA splicing through a novel splicing enhancer and inhibits production of spliced E7 oncogene mRNAs
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- Contribution to journal › Article
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Mark
Regulatory networks and 5' partner usage of miRNA host gene fusions in breast cancer
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- Contribution to journal › Article
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Mark
Thrombotic Risk Determined by Protein C Receptor (PROCR) Variants among Middle-Aged and Older Adults : A Population-Based Cohort Study
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- Contribution to journal › Article
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Mark
N-terminus DUX4-immunohistochemistry is a reliable methodology for the diagnosis of DUX4-fused B-lymphoblastic leukemia/lymphoma (N-terminus DUX4 IHC for DUX4-fused B-ALL)
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- Contribution to journal › Article
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Mark
Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6
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- Contribution to journal › Letter
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Mark
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
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- Contribution to journal › Article