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- 2018
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Mark
The functional 3′-end of immunoglobulin heavy chain variable (IGHV) genes
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- Contribution to journal › Article
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Congenital malformation in offspring of female cancer survivors : A national cohort study
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- Contribution to journal › Article
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Mark
Genetic predisposition to infection in a case of atypical hemolytic uremic syndrome
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- Contribution to journal › Article
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Mark
Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin
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- Contribution to journal › Article
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Mark
Genome-wide analysis yields new loci associating with aortic valve stenosis
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- Contribution to journal › Article
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Mark
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
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- Contribution to journal › Article
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Mark
Internal tandem duplication mutations in the tyrosine kinase domain of FLT3 display a higher oncogenic potential than the activation loop D835Y mutation
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- Contribution to journal › Article
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Mark
Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility
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- Contribution to journal › Article
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Mark
A Single Bout of Electroacupuncture Remodels Epigenetic and Transcriptional Changes in Adipose Tissue in Polycystic Ovary Syndrome
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- Contribution to journal › Article
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Mark
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients
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- Contribution to journal › Article