DiGeorge SyndromeChromosomes, Human, Pair 22Chromosome AberrationsChromosome DisordersSyndromeKaryotypingChromosome DeletionAbnormalities, MultipleCardiovascular AbnormalitiesIn Situ Hybridization, FluorescenceChromosome MappingChromosomesChromosome BandingT-Box Domain ProteinsSex Chromosome AberrationsTruncus Arteriosus, PersistentBranchial RegionTranslocation, GeneticAneuploidyChromosomes, Human, 6-12 and XTrisomyHistone ChaperonesX ChromosomeHypocalcemiaSex ChromosomesChromosomes, Human, 13-15Chromosomes, Human, Pair 13HypoparathyroidismHeart Defects, CongenitalChromosomes, Human, Pair 7Chromosomes, Human, Pair 1Chromosomes, Human, YChromosomes, HumanChromosomes, Human, Pair 21PhenotypeDown SyndromeChromosomes, Human, Pair 11Chromosomes, Human, 21-22 and YChromosomes, Human, 16-18Chromosomes, Human, XMonosomyImmunologic Deficiency SyndromesChromosomes, Human, Pair 18Chromosomes, Human, Pair 17Gene DeletionChromosomes, Human, Pair 6Chromosomes, Human, Pair 9Thymus GlandKlinefelter SyndromeChromosomes, Human, Pair 15CytogeneticsChromosomes, Human, Pair 12Parathyroid GlandsChromosomes, Human, Pair 8MosaicismChromosomes, Human, Pair 2Chromosomes, Human, Pair 14Abnormal KaryotypeChromosome SegregationChromosomes, BacterialMolecular Sequence DataChromosomes, Human, Pair 5Prenatal DiagnosisInfant, NewbornRing ChromosomesNeural CrestMutationChromosome InversionBase SequenceChromosomes, Human, Pair 20Turner SyndromeChromosomes, PlantAmniocentesisEmbryo, MammalianChromosomes, FungalPregnancyGenetic MarkersSex Chromosome Disorders of Sex DevelopmentChromosomes, Human, Pair 16Cytogenetic AnalysisChromosomes, Human, Pair 4Spectral KaryotypingChromosomes, MammalianChromosome PairingPreimplantation DiagnosisChromosomes, Human, Pair 10In Situ HybridizationInfertility, MaleAbortion, HabitualChromosomes, Human, Pair 19Blotting, SouthernChromosomes, Human, 1-3Chromosomes, Artificial, BacterialAorta, ThoracicChromosome Painting22q11 Deletion SyndromeIntellectual DisabilityMetaphase