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Scientific Reports|December 8, 2017
The Genetic Spectrum of Familial Hypercholesterolemia (FH) in the Iranian PopulationR H Fairoozy, M Futema, R Vakili, et al.
American Journal of Epidemiology|April 11, 2001
Ethnic differences in fibrinogen levels: the role of environmental factors and the beta-fibrinogen geneD G Cook, F P Cappuccio, R W Atkinson, et al.
Molecular Biology & Medicine|December 1, 1983
A DNA polymorphism adjacent to the human apolipoprotein CII geneS E Humphries, N I Jowett, L Williams, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|May 1, 1991
Clinical signs of familial hypercholesterolemia in patients with familial defective apolipoprotein B-100 and normal low density lipoprotein receptor functionN B Myant, J J Gallagher, B L Knight, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|November 5, 1997
Apal polymorphism in insulin-like growth factor II (IGF2) gene and weight in middle-aged malesS D O'Dell, G J Miller, J A Cooper, et al.
Human Genetics|March 1, 1987
A common restriction fragment length polymorphism of the human apolipoprotein E gene and its relationship to type III hyperlipidaemiaE C Klasen, P J Talmud, L Havekes, et al.
Annals of Human Genetics|May 1, 1987
The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22M Azoulay, I Henry, F Tata, et al.
Annals of Epidemiology|July 1, 1992
Genetic factors determining thrombosis and fibrinolysisS E Humphries, F R Green, A Temple, et al.
European Journal of Clinical Investigation|August 1, 1996
Lipoprotein lipase gene mutations D9N and N291S in four pedigrees with familial combined hyperlipidaemiaT W de Bruin, F Mailly, H H van Barlingen, et al.
European Journal of Clinical Investigation|March 16, 2002
The effect of the Interleukin-6-174G > C promoter gene polymorphism on endothelial function in healthy volunteersD J Brull, C P M Leeson, H E Montgomery, et al.
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