DiGeorge SyndromeChromosomes, Human, Pair 22SyndromeCardiovascular AbnormalitiesT-Box Domain ProteinsAbnormalities, MultipleChromosome DeletionTruncus Arteriosus, PersistentBranchial RegionHistone ChaperonesHypocalcemiaHypoparathyroidismIn Situ Hybridization, FluorescenceHeart Defects, CongenitalImmunologic Deficiency SyndromesMonosomyDown SyndromeThymus GlandMetabolic Syndrome XGene DeletionParathyroid GlandsPhenotypeNeural CrestNephrotic SyndromeInfant, NewbornChromosome MappingSjogren's SyndromeTranslocation, GeneticAorta, Thoracic