Genome-Wide Linkage Scan for the Metabolic Syndrome in the HERITAGE Family Study - Loos, Ruth J. F.; Katzmarzyk, Peter T.; Rao, D. C.; Rice, Treva; Leon, Arthur S.; Skinner, James S.; Wilmore, Jack H.; Rankinen, Tuomo; Bouchard, Claude (The journal of clinical endocrinology and metabolism, 2003)
Keywords: Adolescent; Adult; African Continental Ancestry Group - genetics; Analysis of Variance; Biological and medical sciences; Cardiovascular diseases; Chromosome 9; Chromosome Mapping; Diabetes mellitus (non-insulin dependent); Environmental factors; European Continental Ancestry Group - genetics; Female; Genetic Linkage; Genome, Human; Genomes; Humans; Linkage analysis; Male; Medical sciences; Metabolic diseases; Metabolic syndrome; Metabolic Syndrome - genetics; Middle Aged; Miscellaneous; Other metabolic disorders; Phenotype; Phenotypes; Phenotypic variations; Principal Component Analysis; Principal components analysis; Quantitative Trait Loci; Risk factors; United States; North America; America; Endocrinopathy; Human; Statistical analysis; Healthy subject; Family study; Negroid; Cardiovascular disease; Metabolic diseases; Genotype; Genetic determinism; Epidemiologic genetics; X Syndrome; Candidate gene; Caucasoid