DiGeorge SyndromeChromosomes, Human, Pair 22ImmunosuppressionSyndromeCardiovascular AbnormalitiesT-Box Domain ProteinsAbnormalities, MultipleChromosome DeletionTruncus Arteriosus, PersistentBranchial RegionHistone ChaperonesHypocalcemiaHypoparathyroidismIn Situ Hybridization, FluorescenceHeart Defects, CongenitalImmunologic Deficiency SyndromesThymus GlandMonosomyImmunosuppressive AgentsParathyroid GlandsGene DeletionNeural CrestPhenotypeImmune ToleranceChromosome MappingInfant, NewbornTranslocation, GeneticAorta, Thoracic