Complement C1qChromosome MappingChromosome DeletionChromosomes, Human, Pair 14Chromosome AberrationsChromosomes, Human, Pair 7Chromosomes, Human, Pair 4Chromosomes, Human, Pair 2Genetic LinkageKaryotypingChromosomes, Human, Pair 10PedigreeChromosome BandingChromosomes, Human, Pair 12Lod ScoreChromosomes, Human, Pair 19Chromosomes, Human, Pair 17Chromosomes, Human, Pair 16UbiquinoneChromosomes, Human, Pair 18Molecular Sequence DataDiGeorge SyndromeMicrosatellite RepeatsAbnormalities, MultipleChromosomes, Human, Pair 9GTP-Binding Protein alpha Subunits, Gq-G11Chromosome DisordersLoss of HeterozygosityMutationGenetic Predisposition to DiseaseQ beta ReplicaseBase SequenceAmino Acid SequencePolymorphism, Single NucleotidePhenotypeComplement Activating EnzymesGenotypeSyndromeChromosomes, Human, Pair 21AllelesComparative Genomic HybridizationGene DosageHaplotypesGenome, HumanDNA, NeoplasmChromosomes, HumanNucleic Acid HybridizationChromosome DuplicationGene DeletionPolymerase Chain ReactionPhysical Chromosome MappingGenetic HeterogeneityGene AmplificationAmino Acid SubstitutionGenome-Wide Association StudyGene RearrangementDNA Mutational AnalysisGenes, DominantMutation, MissenseCytogenetic AnalysisMonosomyHeterozygoteConsanguinityGenetic LociOligodendrogliomaGenes, RecessiveMutagenesis, Site-DirectedCloning, MolecularHomozygoteDNA Copy Number VariationsPolymorphism, GeneticVentilation-Perfusion RatioMyeloid-Lymphoid Leukemia ProteinGlutamineBlotting, SouthernCytogeneticsExonsFaciesProto-OncogenesSequence Homology, Amino AcidCell LineKineticsCase-Control StudiesComplement Pathway, ClassicalGene FrequencyDNA PrimersAllelic ImbalancePoint MutationModels, MolecularSequence Analysis, DNADNA-Binding ProteinsLinkage DisequilibriumProtein BindingSequence DeletionGenetic VariationDNA, SatelliteDNATranscription FactorsGene DuplicationMicrocephaly