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2. Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease

6. A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta

8. A Missense Variant in PLEC Increases Risk of Atrial Fibrillation

9. A rare missense mutation inMYH6confers high risk of coarctation of the aorta

10. Erratum: Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis

11. VariantASGR1Associated with a Reduced Risk of Coronary Artery Disease

12. Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease

13. A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease

14. A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease

15. The structure of the PP2A regulatory subunit B56gamma : The remaining piece of the PP2A jigsaw puzzle

17. Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis

23. Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis

24. Nordic Inheritance Law through the Ages:Spaces of Action and Legal Strategies

26. The structure of the PP2A regulatory subunit B56 gamma: the remaining piece of the PP2A jigsaw puzzle.

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