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Genetics--Periodicals
| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
|---|---|---|---|
| 1 |
Material Type: Article
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International Cooperation to Enable the Diagnosis of All Rare Genetic DiseasesBoycott, Kym M. et al.American journal of human genetics. Volume 100:Issue 5 (2017); pp 695-705 -- Cell Press, Elsevier IncOnline access |
| 2 |
Material Type: Article
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Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple SclerosisManousaki, Despoina et al.American journal of human genetics. Volume 101:Issue 2 (2017); pp 227-238 -- Cell Press, Elsevier IncOnline access |
| 3 |
Material Type: Article
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Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple SclerosisManousaki, Despoina et al.American journal of human genetics. Volume 103:Number 6 (2018, December 6th); pp 1053- -- Cell Press, Elsevier IncOnline access |
| 4 |
Material Type: Article
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A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood PressureSung, Yun J. et al.American journal of human genetics. Volume 102:Number 3 (2018, March 1st); pp 375-400 -- Cell Press, Elsevier IncOnline access |
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- de Mutsert, Renée (3)
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- Noordam, Raymond (3)
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- Mook-Kanamori, Dennis O. (3)
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- GWAS--GxE interactions--lifestyle--blood pressure--multi-ancestry--smoking (1)
- IRDiRC--rare diseases--gene discovery--solving the unsolved--ontologies--Matchmaker Exchange--genome sequencing--transcriptome sequencing--disease modeling (1)
- vitamin D--multiple sclerosis--GWAS--low-frequency genetic variants (1)
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