Cytogenetic AnalysisKaryotypingChromosome AberrationsCytogeneticsChromosome BandingIn Situ Hybridization, FluorescenceTranslocation, GeneticChromosome DisordersTrisomyKaryotypeAneuploidyChromosomes, Human, Pair 7Chromosomes, Human, Pair 11Spectral KaryotypingChromosome DeletionChromosomes, Human, Pair 18Gene RearrangementMonosomyChromosomes, Human, Pair 14Sex Chromosome AberrationsMetaphaseChromosomes, Human, XChromosomes, Human, Pair 13Chromosomes, Human, Pair 5PloidiesChromosomes, Human, Pair 22Chromosome MappingChromosomes, Human, Pair 12Chromosome InversionChromosomes, Human, Pair 3Chromosomes, Human, Pair 9Centralized Hospital ServicesTriploidyX ChromosomeChromosomesChromosomes, Human, 6-12 and XChromosomes, Human, Pair 1Chromosomes, HumanInterphaseMosaicismChromosomes, Human, Pair 8Abnormalities, MultipleMyelodysplastic SyndromesCri-du-Chat SyndromeChromosomes, Human, Pair 17Chromosome BreakageChromosomes, Human, Pair 6Genetic MarkersPrenatal DiagnosisChromosome PaintingChromosomes, Human, Pair 2Nucleic Acid HybridizationRing ChromosomesTurner SyndromeChromosomes, Human, Pair 15Abortion, MissedY ChromosomeLeukemia, MyeloidDNA, NeoplasmSex ChromosomesPhiladelphia ChromosomeChromosomes, Human, Pair 16Chromosomes, Human, Pair 21DiploidyBone MarrowLeukemia, Myelogenous, Chronic, BCR-ABL PositiveImmunophenotypingIntellectual DisabilityComparative Genomic HybridizationDNA ProbesPolyploidyLeukemia, Myeloid, AcuteChromosomes, Human, Pair 4Nucleolus Organizer RegionPrecursor Cell Lymphoblastic Leukemia-LymphomaAbortion, SpontaneousBlotting, SouthernGenes, LethalAzure StainsPolymerase Chain ReactionPhenotypeCentromereChromosomes, Human, 21-22 and YPregnancySyndromeBone Marrow ExaminationDown SyndromeHybrid CellsClone CellsFatal OutcomeMicronucleus TestsGene AmplificationChromosomes, Human, Pair 20HeterochromatinPedigreeChromosomes, Human, Pair 10Sarcoma, SynovialDNA, SatelliteMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, Fusion