Gene DeletionSequence DeletionChromosome DeletionMolecular Sequence DataBase SequenceMutationComplement C1qAmino Acid SequenceChromosome MappingPhenotypeDNA Mutational AnalysisPolymerase Chain ReactionExonsCloning, MolecularPlasmidsClonal DeletionMice, KnockoutPromoter Regions, GeneticTranscription, GeneticAbnormalities, MultipleCell LineChromosomes, Human, Pair 22PedigreeDNA PrimersDiGeorge SyndromeAllelesHomozygoteEscherichia coliMutagenesisRestriction MappingRecombination, GeneticSaccharomyces cerevisiaeBacterial ProteinsIn Situ Hybridization, FluorescenceDNA-Binding Proteins22q11 Deletion SyndromeBlotting, SouthernTranscription FactorsChromosome AberrationsKaryotypingGenotypeGenetic Complementation TestDNAMutagenesis, Site-DirectedRNA, MessengerProtein Structure, TertiarySequence Analysis, DNASyndromeBinding SitesPoint MutationChromosomes, Human, Pair 9HeterozygoteFrameshift MutationSequence Homology, Amino AcidProtein BindingGenes, BacterialMice, Inbred C57BLGene DosageMutagenesis, InsertionalChromosome BandingSaccharomyces cerevisiae ProteinsRepetitive Sequences, Nucleic AcidTransfectionRecombinant Fusion ProteinsChromosomes, Human, Pair 17Chromosome DisordersSequence AlignmentChromosomes, Human, Pair 7GenesGene Expression RegulationGene RearrangementINDEL MutationIntellectual DisabilityComparative Genomic HybridizationLoss of HeterozygosityFungal ProteinsNucleic Acid HybridizationGene Expression Regulation, BacterialDNA Transposable ElementsPolymorphism, GeneticMembrane ProteinsRecombinant ProteinsGenes, FungalChromosomes, Human, Pair 4Nuclear ProteinsCarrier ProteinsMicrosatellite RepeatsCells, CulturedGenetic LinkageSequence Homology, Nucleic AcidModels, GeneticSignal TransductionMultigene FamilyIntronsChromosomes, Human, Pair 16Genes, ViralChromosomes, Human, Pair 10DNA Restriction EnzymesDNA Copy Number VariationsRepressor Proteins