KaryotypeKaryotypingGenomic InstabilityChromosomal InstabilityAbnormal KaryotypeJoint InstabilityChromosome AberrationsMicrosatellite InstabilityChromosome BandingAneuploidyChromosome DisordersTurner SyndromeIn Situ Hybridization, FluorescenceXYY KaryotypeSex Chromosome AberrationsMicrosatellite RepeatsTrisomyTranslocation, GeneticMosaicismCytogenetic AnalysisChromosome PaintingMonosomyChromosomesMutationIsochromosomesCytogeneticsAbnormalities, MultipleSpectral KaryotypingDiploidyChromosome DeletionRing ChromosomesKlinefelter SyndromeLeukemia, Myeloid, AcutePhenotypeChromosomes, HumanDNA, NeoplasmPolyploidyDNA RepairDNA, SatelliteGene RearrangementMutS Homolog 2 ProteinLoss of HeterozygosityChromosome InversionPloidiesSex ChromosomesChromosomes, Human, XChromosomes, Human, 6-12 and XDNA Sequence, UnstableAmniocentesisChromosomes, Human, Pair 13Leukemia, MyeloidNuclear ProteinsTelomereDNA DamageMetaphaseChromosome BreakageChromosomes, Human, YMyelodysplastic SyndromesPregnancyChromosomes, Human, Pair 5Chorionic Villi SamplingChromosomes, Human, Pair 18Chromosome MappingPrognosisPolymerase Chain ReactionBase Pair MismatchBase SequenceChromosomes, Human, Pair 11Trinucleotide RepeatsComparative Genomic HybridizationX ChromosomeDown SyndromeChromosomes, Human, 16-18Colorectal NeoplasmsLigaments, ArticularPrenatal DiagnosisDNA-Binding ProteinsChromosomes, Human, Pair 7Genetic MarkersChromosome FragilityAnkle InjuriesNuchal Translucency MeasurementCell Transformation, NeoplasticMitosisY ChromosomeMolecular Sequence DataShoulder DislocationChromosomes, Human, Pair 22DNA Mismatch RepairIntellectual Disabilityfms-Like Tyrosine Kinase 3Ultrasonography, PrenatalChromosomes, PlantChromosomes, Human, 21-22 and YCell LineChromosome Fragile SitesGonadal DysgenesisCentromereDisorders of Sex DevelopmentFetal Diseases