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Results: 4

Authors: Rabes, JP Varret, M Devillers, M Aegerter, P Villeger, L Krempf, M Junien, C Boileau, C
Citation: Jp. Rabes et al., R3531C mutation in the apolipoprotein B gene is not sufficient to cause hypercholesterolemia, ART THROM V, 20(10), 2000, pp. E76-E82

Authors: Saint-Jore, B Varret, M Dachet, C Rabes, JP Devillers, M Erlich, D Blanchard, P Krempf, M Mathe, D Chanu, B Jacotot, B Farnier, M Bonaiti-Pellie, C Junien, C Boileau, C
Citation: B. Saint-jore et al., Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defects, EUR J HUM G, 8(8), 2000, pp. 621-630

Authors: Thiart, R Varret, M Lintott, CJ Scott, RS Loubser, O du Plessis, L de Villiers, JNP Boileau, C Kotze, MJ
Citation: R. Thiart et al., Mutation analysis in a small cohort of New Zealand patients originating from the United Kingdom demonstrates genetic heterogeneity in familial hypercholesterolemia, MOL CELL PR, 14(5), 2000, pp. 299-304

Authors: Varret, M Rabes, JP Saint-Jore, B Cenarro, A Marinoni, JC Civeira, F Devillers, M Krempf, M Coulon, M Thiart, R Kotze, MJ Schmidt, H Buzzi, JC Kostner, GM Bertolini, S Pocovi, M Rosa, A Farnier, M Martinez, M Junien, C Boileau, C
Citation: M. Varret et al., A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32, AM J HU GEN, 64(5), 1999, pp. 1378-1387
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