22q11 Deletion SyndromeDiGeorge SyndromeChromosomes, Human, Pair 22SyndromeChromosome DeletionVelopharyngeal InsufficiencyGene DeletionAbnormalities, MultipleCraniofacial AbnormalitiesChromosome DisordersSequence DeletionIntellectual DisabilityJacobsen Distal 11q Deletion SyndromeHypoparathyroidismDevelopmental DisabilitiesParietal BoneCri-du-Chat SyndromePhenotypeHemizygoteIn Situ Hybridization, FluorescenceFaciesChromosome BreakageHypocalcemiaCatechol O-MethyltransferaseWAGR SyndromeKaryotypingMuscle HypotoniaSchizophreniaHeart Defects, CongenitalEye AbnormalitiesT-Box Domain ProteinsStanford-Binet TestExostoses, Multiple HereditaryLearning DisordersDown SyndromeMetabolic Syndrome XMutationMolecular Sequence DataMonosomyLanguage Development DisordersComparative Genomic HybridizationChromosome AberrationsPedigreeChromosome BandingChromosome MappingChromosomes, Human, Pair 1Staphylococcus lugdunensisChromosomes, Human, Pair 6Branchial RegionCleft PalateIntelligence TestsGenotypeBase SequenceBrainInfant, NewbornGene DosageNephrotic SyndromeMagnetic Resonance ImagingSiblingsGrowth DisordersSjogren's SyndromeGene RearrangementCognition DisordersTranslocation, GeneticCase-Control StudiesIntelligenceChromosomes, Human, Pair 18Neuropsychological TestsSeizuresGenetic Association StudiesPsychotic DisordersTurner SyndromePsychiatric Status Rating ScalesMyelodysplastic SyndromesAmino Acid SequenceGenetic Predisposition to DiseaseWilliams SyndromeComplement C1qPolymorphism, Single NucleotidePrader-Willi SyndromeCushing SyndromeMice, Inbred C57BLMental DisordersAnalysis of VarianceDNA Mutational AnalysisAcute Coronary SyndromePolycystic Ovary Syndrome