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- 2017
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Mark
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
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- Contribution to journal › Article
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Mark
Gene and miRNA expression profiles in PBMCs from patients with severe and mild emphysema and PiZZ alpha I-antitrypsin deficiency
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- Contribution to journal › Article
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Mark
Heritability of Atrial Fibrillation
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- Contribution to journal › Article
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Mark
Två av tre med bröstcancer valde mutationstestning när alla erbjöds
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts : Comparison with myeloma
(
- Contribution to journal › Article
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Mark
Proteomics insights into infantile neuronal ceroid lipofuscinosis (CLN1) point to the involvement of cilia pathology in the disease
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- Contribution to journal › Article
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Mark
Somatic mutations reveal asymmetric cellular dynamics in the early human embryo
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- Contribution to journal › Article
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Mark
Genredigering-vilka värderingar ska styra?
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- Contribution to journal › Debate/Note/Editorial
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Mark
Hypertension reduces soluble guanylyl cyclase expression in the mouse aorta via the Notch signaling pathway
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- Contribution to journal › Article
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Mark
Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility
(
- Contribution to journal › Article