MonosomyKaryotypeKaryotypingAbnormal KaryotypeChromosome AberrationsChromosome DisordersTrisomyChromosomes, Human, Pair 7Chromosome BandingTurner SyndromeIn Situ Hybridization, FluorescenceChromosome DeletionChromosomes, Human, Pair 3Translocation, GeneticUveal NeoplasmsAneuploidyAbnormalities, MultipleSex Chromosome AberrationsChromosomes, Human, Pair 21Cytogenetic AnalysisRing ChromosomesChromosomes, Human, 16-18MosaicismChromosomes, Human, 6-12 and XChromosomes, Human, 21-22 and YMyelodysplastic SyndromesXYY KaryotypeIsochromosomesChoroid NeoplasmsChromosomes, Human, Pair 13CytogeneticsChromosomes, Human, Pair 22Chromosomes, Human, Pair 5Chromosomes, Human, Pair 8Chromosomes, Human, Pair 1Leukemia, Myeloid, AcuteChromosomes, Human, XIntellectual DisabilityChromosomes, Human, Pair 18Chromosomes, Human, 1-3Chromosomes, Human, 13-15Chromosomes, Human, Pair 10Chromosomes, Human, Pair 14Chromosome PaintingChromosome InversionChromosomes, Human, Pair 9DiploidyDown SyndromeChromosome MappingChromosomes, Human, Pair 6Chromosomes, HumanX ChromosomeLeukemia, MyeloidChromosomes, Human, Pair 11Comparative Genomic HybridizationChromosomesKlinefelter SyndromeSyndromeAnemia, RefractoryFacial BonesChromosomes, Human, Pair 16MelanomaAbortion, SpontaneousAnemia, Refractory, with Excess of BlastsDermatoglyphicsHoloprosencephalyChromosomes, Human, Pair 17Pregnancy