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A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.
Francke S, Manraj M, Lacquemant C, Lecoeur C, Leprêtre F, Passa P, Hebe A, Corset L, Yan SL, Lahmidi S, Jankee S, Gunness TK, Ramjuttun US, Balgobin V, Dina C, Froguel P. Francke S, et al. Among authors: passa p. Hum Mol Genet. 2001 Nov 15;10(24):2751-65. doi: 10.1093/hmg/10.24.2751. Hum Mol Genet. 2001. PMID: 11734540
Association between high von willebrand factor levels and the Thr789Ala vWF gene polymorphism but not with nephropathy in type I diabetes. The GENEDIAB Study Group and the DESIR Study Group.
Lacquemant C, Gaucher C, Delorme C, Chatellier G, Gallois Y, Rodier M, Passa P, Balkau B, Mazurier C, Marre M, Froguel P. Lacquemant C, et al. Among authors: passa p. Kidney Int. 2000 Apr;57(4):1437-43. doi: 10.1046/j.1523-1755.2000.00988.x. Kidney Int. 2000. PMID: 10760079 Free article.
[Diabetes and heredity].
Froguel P, Passa P. Froguel P, et al. Among authors: passa p. Rev Med Interne. 1991 Mar-Apr;12(2):123-7. doi: 10.1016/s0248-8663(05)81375-x. Rev Med Interne. 1991. PMID: 1852994 Review. French.
264 results