KaryotypeKaryotypingAbnormal KaryotypeChromosome AberrationsChromosome BandingTurner SyndromeXYY KaryotypeChromosome DisordersSex Chromosome AberrationsTrisomyIn Situ Hybridization, FluorescenceMosaicismTranslocation, GeneticMonosomyCytogenetic AnalysisAneuploidyChromosome PaintingIsochromosomesDisabled PersonsCytogeneticsAbnormalities, MultipleChromosomesKlinefelter SyndromeLeukemia, Myeloid, AcuteRing ChromosomesSpectral KaryotypingDiploidyChromosome DeletionChromosomes, Human, 6-12 and XAmniocentesisSex ChromosomesChromosome InversionLeukemia, MyeloidPregnancyChromosomes, Human, XChorionic Villi SamplingMyelodysplastic SyndromesIntellectual DisabilityChromosomes, Human, YChromosomes, Human, 16-18Down SyndromeChromosomes, Human, Pair 13Prenatal DiagnosisNuchal Translucency Measurementfms-Like Tyrosine Kinase 3Chromosomes, Human, Pair 5Y ChromosomeUltrasonography, PrenatalChromosomes, Human, 21-22 and YChromosomes, HumanChromosomes, Human, Pair 18X ChromosomeDisorders of Sex DevelopmentGene RearrangementFetal DiseasesChromosomes, Human, Pair 21Chromosomes, Human, Pair 7PolyploidyChromosomes, PlantGonadal Dysgenesis, 46,XYNucleolus Organizer RegionChromosomes, Human, Pair 11MetaphaseChromosomes, Human, 4-5Sex ChromatinPrognosisPregnancy Trimester, FirstChromosome MappingPloidiesChromosomes, Human, Pair 22Chromosomes, Human, 1-3Risk FactorsHomeless PersonsGonadal DysgenesisUnited StatesChromosomes, Human, 13-15Abortion, HabitualSex Chromosome DisordersPhenotypeAbortion, SpontaneousInfant, NewbornSex Chromosome Disorders of Sex DevelopmentComparative Genomic HybridizationChromosomes, Human, Pair 14GonadoblastomaMentally Ill PersonsChromosomes, Human, Pair 8Visually Impaired PersonsMentally Disabled PersonsSyndromeLiliaceaeChromosomes, Human, Pair 12Acute DiseaseTetraploidyGenetic MarkersAge FactorsRetrospective StudiesTandem Repeat SequencesDNA, FungalTriploidy