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A genome-wide RNAi screen identifies regulators of cholesterol-modified hedge...
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Genetic ancestry and lower extremity peripheral artery disease in the Multi-E...
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Thrombin generation in first-degree relatives of patients with venous thrombo...
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Are autoimmune diseases predictable?
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Disclosing results to genomic research participants: differences that matter.
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Identification of VPS35 mutations replicated in French families with Parkinso...
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On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European popula...
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Detection of high-risk atherosclerotic plaque: report of the NHLBI Working Gr...
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Detection of BRCA1/2 mutations in breast cancer patients from Thailand and Pa...
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Parental electrocardiographic screening identifies a high degree of inheritan...
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Advising a cardiac disease gene positive yet phenotype negative or borderline...
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Significance of deep T-wave inversions in asymptomatic athletes with normal c...
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C9ORF72 repeat expansions in the frontotemporal dementias spectrum of disease...
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Mutations of the ANG gene in French patients with sporadic amyotrophic latera...
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Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
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Spectrum of mutations in Gitelman syndrome.
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Complement genes strongly predict recurrence and graft outcome in adult renal...
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The significance of MEN1 mutations in pituitary carcinomas.
International audience
