Sequence DeletionMolecular Sequence DataBase SequenceSyndromeGene DeletionChromosome DeletionDown SyndromeMetabolic Syndrome XMutationNephrotic SyndromeSjogren's SyndromeAbnormalities, MultipleDiGeorge SyndromeTurner SyndromeMyelodysplastic SyndromesPhenotypeWilliams SyndromeAmino Acid SequencePrader-Willi SyndromeCushing SyndromeAcute Coronary SyndromePolycystic Ovary SyndromePedigreeDNA Mutational AnalysisLong QT SyndromeHorner SyndromeIntellectual DisabilityChromosomes, Human, Pair 22Chromosome MappingGuillain-Barre SyndromeHemolytic-Uremic SyndromePolymerase Chain ReactionAngelman SyndromeCompartment SyndromesTourette SyndromeExonsAntiphospholipid SyndromePorcine Reproductive and Respiratory SyndromeKlinefelter SyndromeWerner SyndromeCarpal Tunnel SyndromeMice, KnockoutBartter SyndromePorcine respiratory and reproductive syndrome virusReye SyndromeFaciesEhlers-Danlos SyndromeHELLP SyndromeBloom SyndromeHomozygoteBrugada SyndromeCell LineCloning, MolecularRespiratory Distress Syndrome, AdultGenotypeIn Situ Hybridization, FluorescencePlasmidsAllelesHeterozygotePromoter Regions, GeneticCraniofacial AbnormalitiesSevere Acute Respiratory SyndromeTranscription, GeneticDNA PrimersWiskott-Aldrich SyndromeClonal DeletionRestless Legs SyndromeKaryotypingFrameshift MutationJob SyndromeParaneoplastic SyndromesDNA-Binding ProteinsSweet SyndromeTranscription Factors