KaryotypeKaryotypingAbnormal KaryotypeChromosome AberrationsChromosome BandingTurner SyndromeXYY KaryotypeChromosome DisordersSex Chromosome AberrationsTrisomyIn Situ Hybridization, FluorescenceMosaicismTranslocation, GeneticMonosomyCytogenetic AnalysisAneuploidyChromosome PaintingIsochromosomesChromosomesCytogeneticsAbnormalities, MultipleKlinefelter SyndromeLeukemia, Myeloid, AcuteRing ChromosomesSpectral KaryotypingDiploidyChromosome DeletionPregnancySex ChromosomesChromosomes, Human, 6-12 and XAmniocentesisChromosome InversionChromosomes, Human, XLeukemia, MyeloidChorionic Villi SamplingChromosomes, Human, YMyelodysplastic SyndromesChromosomes, Human, 16-18Chromosomes, Human, Pair 13PhenotypeDown SyndromeNuchal Translucency MeasurementPrenatal DiagnosisY ChromosomeX ChromosomeChromosomes, Human, Pair 5Gene RearrangementChromosome MappingPolyploidyDisorders of Sex DevelopmentUltrasonography, Prenatalfms-Like Tyrosine Kinase 3Chromosomes, HumanChromosomes, Human, Pair 18Chromosomes, Human, 21-22 and YIntellectual DisabilityChromosomes, Human, Pair 21Fetal DiseasesPhylogenyChromosomes, Human, Pair 7Chromosomes, PlantMutationChromosomes, Human, Pair 11Evolution, MolecularMetaphaseNucleolus Organizer RegionGonadal Dysgenesis, 46,XYPloidiesChromosomes, Human, Pair 22Pregnancy Trimester, FirstSex ChromatinChromosomes, Human, 4-5Gonadal DysgenesisSpecies SpecificityPrognosisChromosomes, Human, 1-3Abortion, HabitualAbortion, SpontaneousMolecular Sequence DataChromosomes, Human, 13-15Biological EvolutionSex Chromosome DisordersComparative Genomic HybridizationGenetic VariationSex Chromosome Disorders of Sex DevelopmentTime FactorsChromosomes, Human, Pair 14Base SequenceChromosomes, Human, Pair 8Cell LineGonadoblastomaGenetic MarkersInfant, NewbornSyndromeTetraploidyLiliaceaeCells, CulturedChromosomes, Human, Pair 12DNA, FungalAcute Disease