Alu ElementsGene DeletionSequence DeletionChromosome DeletionBase SequenceMolecular Sequence DataRepetitive Sequences, Nucleic AcidMutationLong Interspersed Nucleotide ElementsAmino Acid SequenceExonsGenome, HumanPolymerase Chain ReactionChromosome MappingCloning, MolecularShort Interspersed Nucleotide ElementsDNATranscription, GeneticSequence Homology, Nucleic AcidMutagenesis, InsertionalPhenotypePromoter Regions, GeneticDNA Transposable ElementsDNA Mutational AnalysisPlasmidsChromosomes, Human, Pair 22Restriction MappingCell LineRecombination, GeneticDNA PrimersPrimatesIntronsClonal DeletionSequence Analysis, DNAGenesSignal Recognition ParticleMice, KnockoutRetroelementsAllelesBlotting, SouthernRNA, MessengerSequence AlignmentPolymorphism, GeneticIn Situ Hybridization, FluorescenceEscherichia coliEvolution, MolecularMutagenesisHomozygoteTranscription FactorsSaccharomyces cerevisiaeDNA-Binding ProteinsGene Expression RegulationBinding SitesPedigreeHeLa CellsDNA Restriction EnzymesGene Rearrangement22q11 Deletion SyndromeRNA Polymerase IIIMultigene FamilyRNABacterial ProteinsHominidaeTransfectionAbnormalities, MultipleModels, GeneticRNA EditingGenetic VariationNucleic Acid HybridizationBlood Buffy CoatProtein BindingGenotypeGenetic Complementation TestPoint MutationRNA, Small CytoplasmicProtein Structure, TertiaryChromosome BreakageDiGeorge SyndromeFrameshift MutationSaccharomyces cerevisiae ProteinsSequence Homology, Amino AcidHeterozygoteMice, Inbred C57BLGenes, BacterialNucleic Acid ConformationMutagenesis, Site-DirectedGenetic MarkersGene DosageRecombinant Fusion ProteinsPan troglodytesConsensus SequenceChromosomes, Human, Pair 9Syndrome3' Flanking RegionNuclear ProteinsRNA-Binding ProteinsIntellectual DisabilityINDEL MutationCells, CulturedPhylogeny