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  • A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses
    [作者:Ripatti, S; Tikkanen, E; Orho-Melander, M; Havulinna, AS; Silander, K; Sharma, A; Guiducci, C; Perola, M; Jula, A; Sinisalo, J; Lokki, ML; Nieminen, MS; Melander, O; Salomaa, V; Peltonen, L; Kathiresan, S,期刊:Lancet, 页码:1393-1400 , 文章类型: Article,,卷期:2010年376-9750]
  • Background Comparison of patients with coronary heart disease and controls in genome-wide association studies has revealed several single nucleotide polymorphisms (SNPs) associated with coronary heart disease. We aimed t...
  • Escherichia coli O157
    [作者:Pennington, H,期刊:Lancet, 页码:1428-1435 , 文章类型: Review,,卷期:2010年376-9750]
  • Escherichia coil 0157 is an uncommon but serious cause of gastroenteritis. This bacterium is noteworthy because a few, but significant, number of infected people develop the haemolytic uraemic syndrome, which is the most...
  • Phenylketonuria
    [作者:Blau, N; van Spronsen, FJ; Levy, HL,期刊:Lancet, 页码:1417-1427 , 文章类型: Article,,卷期:2010年376-9750]
  • Phenylketonuria is the most prevalent disorder caused by an inborn error in aminoacid metabolism. It results from mutations in the phenylalanine hydroxylase gene. Phenotypes can vary from a very mild increase in blood ph...