KaryotypingKaryotypeChromosome AberrationsAbnormal KaryotypeMonosomyCytogenetic AnalysisIsochromosomesIn Situ Hybridization, FluorescenceCytogeneticsChromosome BandingTranslocation, GeneticAnemia, Refractory, with Excess of BlastsLeukemia, Myeloid, AcuteChromosomes, Human, Pair 5Myelodysplastic SyndromesLeukemia, MyeloidChromosomes, Human, Pair 11Chromosomes, Human, Pair 14Chromosome DeletionChromosomes, Human, Pair 8Chromosomes, Human, Pair 17PrognosisImmunophenotypingAcute DiseaseSurvival AnalysisTurner SyndromeXYY KaryotypeChromosome DisordersSurvival RateSex Chromosome AberrationsTrisomyMosaicismAneuploidyChromosome PaintingAbnormalities, MultipleChromosomesKlinefelter SyndromeRing ChromosomesSpectral KaryotypingDiploidyChromosomes, Human, 6-12 and XAmniocentesisSex ChromosomesChromosome InversionChromosomes, Human, XChorionic Villi SamplingChromosomes, Human, 16-18PregnancyChromosomes, Human, YChromosomes, Human, Pair 13Nuchal Translucency MeasurementPrenatal DiagnosisDown Syndromefms-Like Tyrosine Kinase 3Y ChromosomeUltrasonography, PrenatalChromosomes, Human, 21-22 and YChromosomes, Human, Pair 18Disorders of Sex DevelopmentGene RearrangementChromosomes, HumanX ChromosomeFetal DiseasesChromosomes, Human, Pair 21PolyploidyIntellectual DisabilityChromosomes, Human, Pair 7Chromosomes, PlantGonadal Dysgenesis, 46,XYNucleolus Organizer RegionMetaphaseChromosomes, Human, 4-5Sex ChromatinPregnancy Trimester, FirstPloidiesChromosomes, Human, Pair 22Chromosomes, Human, 1-3Gonadal DysgenesisChromosome MappingChromosomes, Human, 13-15Abortion, HabitualSex Chromosome DisordersAbortion, SpontaneousSex Chromosome Disorders of Sex DevelopmentComparative Genomic HybridizationGonadoblastomaPhenotypeLiliaceaeTetraploidyChromosomes, Human, Pair 12Genetic MarkersSyndromeTriploidyDNA, FungalTandem Repeat SequencesChromosomes, Human, 19-20Chromosomes, FungalAzure StainsCentromerePregnancy Trimester, Second