Gonadal Dysgenesis, 46,XYKaryotypeGonadal Dysgenesis, MixedKaryotypingDisorders of Sex DevelopmentAndrogen-Insensitivity SyndromeSex Chromosome AberrationsGonadal DysgenesisMosaicismY ChromosomeAbnormal Karyotype46, XY Disorders of Sex DevelopmentChromosome AberrationsChromosome BandingXYY KaryotypeTurner SyndromeChromosome DisordersTrisomyIn Situ Hybridization, FluorescenceTranslocation, GeneticAneuploidyMonosomySex ChromosomesCytogenetic AnalysisKlinefelter SyndromeChromosome PaintingAbnormalities, MultipleX ChromosomeIsochromosomesSex-Determining Region Y ProteinCytogeneticsRing ChromosomesChromosomesSex Determination ProcessesChromosomes, Human, XChromosomes, Human, 6-12 and XLeukemia, Myeloid, AcuteChromosomes, Human, YSpectral KaryotypingChromosome DeletionGonadoblastomaDiploidyAmniocentesisChromosomes, Human, 16-18Chromosome InversionGenes, sryOvotesticular Disorders of Sex DevelopmentChromosomes, Human, Pair 13Chromosomes, Human, 21-22 and YSex ChromatinPregnancySex Chromosome Disorders of Sex DevelopmentLeukemia, MyeloidChorionic Villi SamplingPrenatal DiagnosisChromosomes, Human, 13-15Chromosomes, Human, 4-5Chromosomes, Human, Pair 18Sex Determination AnalysisSex Chromosome DisordersDown SyndromeIntellectual DisabilityMyelodysplastic SyndromesChromosomes, Human, 1-3Chromosomes, Human, Pair 21Chromosomes, Human, Pair 5Nuchal Translucency MeasurementPhenotypeUltrasonography, PrenatalChromosomes, HumanChromosomes, Human, Pair 7Gene RearrangementMetaphaseChromosome Mappingfms-Like Tyrosine Kinase 3TestisChromosomes, Human, Pair 11Sexual DevelopmentChromosomes, Human, Pair 22Fetal DiseasesPolyploidyChromosomes, PlantMeiosisNucleolus Organizer RegionComparative Genomic HybridizationChimeraPregnancy Trimester, FirstPloidiesInfertility, MaleChromosomes, Human, Pair 14Frasier SyndromeGonadsAbortion, HabitualChromosomes, Human, Pair 8Abortion, Spontaneous