Cardiovascular DiseasesChromosomesChromosome MappingX ChromosomeChromosome BandingChromosome AberrationsChromosomes, Human, Pair 1Sex ChromosomesChromosomes, HumanGenetic LociChromosomes, BacterialChromosomes, Human, Pair 7Chromosome SegregationChromosomes, Human, Pair 11Chromosomes, Human, Pair 17Risk FactorsChromosomes, Human, Pair 9Chromosomes, Human, Pair 6Chromosome DeletionChromosomes, Human, Pair 21Genetic LinkageChromosomes, FungalChromosomes, Human, Pair 2Chromosomes, PlantChromosomes, Human, 6-12 and XChromosomes, MammalianChromosomes, Human, Pair 16Chromosomes, Human, Pair 13Chromosomes, Human, Pair 22Chromosomes, Human, Pair 4Chromosomes, Human, Pair 10Quantitative Trait LociChromosomes, Human, Pair 19Chromosome PairingChromosomes, Human, Pair 8Genetic MarkersChromosomes, Artificial, BacterialChromosomes, Human, Pair 12Chromosomes, Human, YChromosomes, Human, Pair 5Chromosome DisordersChromosomes, Human, XChromosomes, Human, Pair 15Chromosomes, Human, 1-3Chromosome PaintingChromosomes, Human, Pair 14KaryotypingIn Situ Hybridization, FluorescenceChromosomes, Human, Pair 18Chromosomes, Artificial, YeastMolecular Sequence DataChromosomes, Human, 16-18Chromosomes, Human, Pair 20Chromosomes, Human, 13-15Base SequenceChromosome BreakageChromosomes, Human, 21-22 and YPhenotypeChromosome InversionRing ChromosomesMicrosatellite RepeatsGenotypeCrosses, GeneticLod ScoreChromosomes, Human, 4-5Chromosome PositioningMutationPedigreeHypertensionRecombination, GeneticCohort StudiesX Chromosome InactivationCentromereTranslocation, GeneticAtherosclerosisHybrid CellsPolymorphism, GeneticChromosomes, InsectGenetic Predisposition to DiseaseChromosome StructuresBiological MarkersPolymorphism, Single NucleotideGenetic VariationMeiosisBlood PressureChromosomes, Human, 19-20Models, GeneticRisk AssessmentAneuploidyMitosisProspective StudiesMetaphaseObesityDiabetes Mellitus, Type 2Cloning, MolecularMetabolic Syndrome XSequence Analysis, DNAFollow-Up StudiesAllelesAmino Acid Sequence