KaryotypingKaryotypeAbnormal KaryotypeChromosome BandingPrimed In Situ LabelingChromosome AberrationsLarixTrisomyCytogeneticsAneuploidyIn Situ Hybridization, FluorescenceChromosome DisordersCytogenetic AnalysisTurner SyndromeChromosomes, Human, 16-18MosaicismSex Chromosome AberrationsChromosomesTranslocation, GeneticChromosome DeletionChromosomes, Human, YAbnormalities, MultipleInfertility, MaleChromosome MappingDNA, RibosomalPhenotypeXYY KaryotypeMonosomyChromosome PaintingIsochromosomesKlinefelter SyndromeLeukemia, Myeloid, AcuteRing ChromosomesSpectral KaryotypingDiploidyChromosomes, Human, 6-12 and XAmniocentesisSex ChromosomesChromosome InversionLeukemia, MyeloidChromosomes, Human, XChorionic Villi SamplingMyelodysplastic SyndromesPregnancyChromosomes, 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 DysgenesisChromosomes, Human, 13-15Abortion, HabitualSex Chromosome DisordersAbortion, SpontaneousSex Chromosome Disorders of Sex DevelopmentPrognosisComparative Genomic HybridizationChromosomes, Human, Pair 14GonadoblastomaChromosomes, Human, Pair 8