Phenotypic, genetic, and genome-wide structure in the metabolic syndrome.

BMC genetics

Volumn 4 Suppl 1, Issue , 2003, Pages

  Martin, Lisa J ^a   North, Kari E ^b   Dyer, Tom ^b   Blangero, John ^b   Comuzzie, Anthony G ^b   Williams, Jeff ^b  

^a CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

CHOLESTEROL; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; TRIACYLGLYCEROL;

ADULT; ADULT CHILD; ARTICLE; BLOOD; BLOOD PRESSURE; BODY MASS; CARDIOVASCULAR DISEASE; CHROMOSOME MAP; COHORT ANALYSIS; FEMALE; GENETICS; GENOTYPE; HUMAN; HUMAN GENOME; MALE; METABOLIC SYNDROME X; METHODOLOGY; MIDDLE AGED; PATHOLOGY; PATHOPHYSIOLOGY; PHENOTYPE; PHYSIOLOGY;

ADULT; ADULT CHILDREN; BLOOD PRESSURE; BODY MASS INDEX; CARDIOVASCULAR DISEASES; CHOLESTEROL; CHOLESTEROL, HDL; CHROMOSOME MAPPING; COHORT STUDIES; FEMALE; GENOME, HUMAN; GENOTYPE; HUMANS; MALE; METABOLIC SYNDROME X; MIDDLE AGED; PHENOTYPE; TRIGLYCERIDES;

EID: 34248671650     PISSN: None     EISSN: 14712156     Source Type: Journal    
DOI: 10.1186/1471-2156-4-s1-s95     Document Type: Article

References (0)