Cytogenetic AnalysisKaryotypingChromosome AberrationsCytogeneticsChromosome BandingIn Situ Hybridization, FluorescenceTranslocation, GeneticDNA ProbesChromosome DisordersTrisomyKaryotypeAneuploidyChromosomes, Human, Pair 7Chromosomes, Human, Pair 11Chromosome DeletionSpectral KaryotypingMolecular ProbesGene RearrangementChromosomes, Human, Pair 18MonosomyChromosomes, Human, Pair 14Sex Chromosome AberrationsMetaphaseChromosome MappingChromosomes, Human, XChromosomes, Human, Pair 13Chromosomes, Human, Pair 22Chromosomes, Human, Pair 5PloidiesNucleic Acid HybridizationChromosomes, Human, Pair 12Chromosome InversionChromosomes, Human, Pair 3Chromosomes, Human, Pair 9Centralized Hospital ServicesOligonucleotide ProbesX ChromosomeChromosomesChromosomes, Human, 6-12 and XTriploidyChromosomes, Human, Pair 1Chromosomes, HumanInterphaseMosaicismChromosomes, Human, Pair 8Abnormalities, MultipleMyelodysplastic SyndromesChromosomes, Human, Pair 17Genetic MarkersChromosome PaintingChromosome BreakageCri-du-Chat SyndromeChromosomes, Human, Pair 6Prenatal DiagnosisChromosomes, Human, Pair 2Molecular Probe TechniquesY ChromosomeRing ChromosomesChromosomes, Human, Pair 15DNA, NeoplasmTurner SyndromePolymerase Chain ReactionAbortion, MissedLeukemia, MyeloidChromosomes, Human, Pair 16Chromosomes, Human, Pair 21Blotting, SouthernSex ChromosomesPhiladelphia ChromosomeDiploidyBone MarrowLeukemia, Myelogenous, Chronic, BCR-ABL PositiveComparative Genomic HybridizationIntellectual DisabilityBase SequenceImmunophenotypingRNA ProbesPolyploidyChromosomes, Human, Pair 4Nucleolus Organizer RegionLeukemia, Myeloid, AcutePrecursor Cell Lymphoblastic Leukemia-LymphomaMolecular Sequence DataPhenotypeAbortion, SpontaneousDNAAzure StainsGenes, LethalCentromereHybrid CellsPregnancyGene AmplificationSyndromeChromosomes, Human, 21-22 and YNucleic Acid ProbesClone CellsDown SyndromeBone Marrow ExaminationMicronucleus TestsPedigree