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Results: 1-4 |
Results: 4

Authors: Clee, SM Loubser, O Collins, J Kastelein, JJP Hayden, MR
Citation: Sm. Clee et al., The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery disease, CLIN GENET, 60(4), 2001, pp. 293-300

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: Brooks-Wilson, A Marcil, M Clee, SM Zhang, LH Roomp, K van Dam, M Yu, L Brewer, C Collins, JA Molhuizen, HOF Loubser, O Ouelette, BFF Fichter, K Ashbourne-Excoffon, KJD Sensen, CW Scherer, S Mott, S Denis, M Martindale, D Frohlich, J Morgan, K Koop, B Pimstone, S Kastelein, JJP Genest, J Hayden, MR
Citation: A. Brooks-wilson et al., Mutations in ABC1 in Tangier disease and familial high-density lipoproteindeficiency, NAT GENET, 22(4), 1999, pp. 336-345

Authors: Loubser, O Marais, AD Kotze, MJ Godenir, N Thiart, R Scholtz, CL de Villiers, JNP Hillermann, R Firth, JC Weich, HFH Maritz, F Jones, S van der Westhuyzen, DR
Citation: O. Loubser et al., Founder mutations in the LDL receptor gene contribute significantly to thefamilial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry, CLIN GENET, 55(5), 1999, pp. 340-345
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