KaryotypeKaryotypingAbnormal KaryotypeChromosome AberrationsChromosome BandingTurner SyndromeXYY KaryotypeChromosome DisordersSex Chromosome AberrationsTrisomyIn Situ Hybridization, FluorescenceMosaicismTranslocation, GeneticMonosomyCytogenetic AnalysisAneuploidyChromosome PaintingIsochromosomesCytogeneticsAbnormalities, MultipleChromosomesKlinefelter SyndromeLeukemia, Myeloid, AcuteRing ChromosomesSpectral KaryotypingDiploidyChromosome DeletionChromosomes, Human, 6-12 and XAmniocentesisSex ChromosomesChromosome InversionLeukemia, MyeloidChromosomes, Human, XChorionic Villi SamplingMyelodysplastic SyndromesChromosomes, Human, 16-18PregnancyChromosomes, Human, YChromosomes, Human, Pair 13Nuchal Translucency MeasurementPrenatal DiagnosisDown Syndromefms-Like Tyrosine Kinase 3Chromosomes, Human, Pair 5Y 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 RegionChromosomes, Human, Pair 11MetaphaseChromosomes, 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 DevelopmentPrognosisComparative Genomic HybridizationChromosomes, Human, Pair 14GonadoblastomaChromosomes, Human, Pair 8PhenotypeLiliaceaeTetraploidyChromosomes, Human, Pair 12Genetic MarkersSyndromeTriploidyDNA, FungalTandem Repeat SequencesChromosomes, Human, 19-20Chromosomes, FungalAzure StainsCentromerePregnancy Trimester, SecondXenarthraInfertility, MaleInfant, NewbornChromosomes, Human, Pair 9Ovotesticular Disorders of Sex DevelopmentAcute Disease