PhenotypeSyndromeChromosomes, Human, Pair 21Upper Extremity Deformities, CongenitalDown SyndromeAbnormalities, MultipleAntley-Bixler Syndrome PhenotypeLimb Deformities, CongenitalTrisomyIntellectual DisabilityKaryotypingChromosome DeletionIn Situ Hybridization, FluorescencePedigreeChromosome MappingMutationGenotypeDisease Models, AnimalMetabolic Syndrome XNephrotic SyndromeSjogren's SyndromeTurner SyndromeMolecular Sequence DataMyelodysplastic SyndromesCushing SyndromePolycystic Ovary SyndromeWilliams SyndromeAcute Coronary SyndromeDiGeorge SyndromePrader-Willi SyndromeLong QT SyndromeBase SequenceHorner SyndromeGuillain-Barre SyndromeHemolytic-Uremic SyndromeTourette SyndromeCompartment SyndromesAmino Acid SequenceAntiphospholipid SyndromeKlinefelter SyndromeAllelesWerner SyndromePorcine Reproductive and Respiratory SyndromeDNA Mutational AnalysisBartter SyndromeCarpal Tunnel SyndromeReye SyndromePorcine respiratory and reproductive syndrome virusBloom SyndromeAngelman SyndromeEhlers-Danlos SyndromeBrugada SyndromeHELLP SyndromeMice, Inbred C57BLCells, CulturedMutation, MissenseGene DeletionHeterozygoteMice, KnockoutRespiratory Distress Syndrome, AdultFaciesWiskott-Aldrich SyndromeJob SyndromeCell DifferentiationSevere Acute Respiratory SyndromeTime FactorsHomozygoteRestless Legs SyndromeCraniofacial AbnormalitiesSignal TransductionMice, TransgenicAcquired Immunodeficiency SyndromeParaneoplastic SyndromesRNA, MessengerGenetic LinkageSweet SyndromeTranscription FactorsRisk FactorsEye AbnormalitiesCell LinePolymerase Chain ReactionKallmann SyndromeGenes, RecessiveChurg-Strauss SyndromeSturge-Weber SyndromeInfant, NewbornGenetic Predisposition to DiseaseGenetic Complementation TestChediak-Higashi SyndromeBudd-Chiari SyndromeGenes, DominantBardet-Biedl SyndromePregnancyUsher SyndromesGene Expression RegulationCase-Control StudiesSezary SyndromeTreatment OutcomeGene ExpressionWolff-Parkinson-White Syndrome