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At-home genetic tests : a healthy dose of skepticism may be the best prescription / produced in cooperation with the Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC).

[Washington, D.C.] : Federal Trade Commission, Bureau of Consumer Protection, Division of Consumer and Business Education, [2006]

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Partial complex I deficiency due to the CNS conditional ablation of Ndufa5 results in a mild chronic encephalopathy but no increase in oxidative damage

Peralta, Susana

Human molecular genetics volume 23 issue 6 page 1399 -- Oxford University Press

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CLYBL is a polymorphic human enzyme with malate synthase and β-methylmalate synthase activity

Strittmatter, Laura

Human molecular genetics volume 23 issue 9 page 2313 -- Oxford University Press

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A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort

Nag, Abhishek

Human molecular genetics volume 23 issue 12 page 3343 -- Oxford University Press

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Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity

Pei, Yu-Fang

Human molecular genetics volume 23 issue 3 page 820 -- Oxford University Press

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Human molecular genetics volume 23 issue 3 page NP -- Oxford University Press

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Connexin defects underlie arrhythmogenic right ventricular cardiomyopathy in a novel mouse model

Lyon, Robert C.

Human molecular genetics volume 23 issue 5 page 1134 -- Oxford University Press

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Restoration of muscle strength in dystrophic muscle by angiotensin-1-7 through inhibition of TGF-β signalling

Acuña, María José

Human molecular genetics volume 23 issue 5 page 1237 -- Oxford University Press

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ACAD9, a complex I assembly factor with a moonlighting function in fatty acid oxidation deficiencies

Nouws, Jessica

Human molecular genetics volume 23 issue 5 page 1311 -- Oxford University Press

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Identification and analysis of large intergenic non-coding RNAs regulated by p53 family members through a genome-wide analysis of p53-binding sites

Idogawa, Masashi

Human molecular genetics volume 23 issue 11 page 2847 -- Oxford University Press

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