KaryotypingKaryotypeSpectral KaryotypingAbnormal KaryotypeChromosome AberrationsChromosome DisordersIn Situ Hybridization, FluorescenceTrisomyChromosome BandingAneuploidyAmniocentesisPrenatal DiagnosisCytogenetic AnalysisCytogeneticsSex Chromosome AberrationsChromosome PaintingTranslocation, GeneticTurner SyndromeFetal DiseasesDown SyndromeChorionic Villi SamplingRing ChromosomesAbnormalities, MultipleUltrasonography, PrenatalMosaicismSex Chromosome DisordersChromosomes, HumanPregnancyChromosomes, Human, Pair 13Chromosomes, Human, Pair 18MonosomyComparative Genomic HybridizationChromosome DeletionChromosomesXYY KaryotypeNeckPregnancy Trimester, FirstKlinefelter SyndromeAzure StainsChromosomes, Human, Pair 7Chromosomes, Human, Pair 20Nuchal Translucency MeasurementMetaphaseChromosomes, Human, XIntellectual DisabilityChromosomes, Human, YAbortion, HabitualChromosomes, Human, Pair 5Pregnancy, High-RiskGene RearrangementMyelodysplastic SyndromesLeukemia, Myeloid, AcuteChromosomes, Human, Pair 21DiploidyPregnancy Trimester, SecondMaternal AgeSex Chromosome Disorders of Sex DevelopmentChromosome InversionNucleic Acid HybridizationChromosomes, Human, Pair 14Uniparental DisomySex ChromosomesNectriaIsochromosomesAbortion, SpontaneousMycological Typing TechniquesCrown-Rump LengthAzoospermiaGenetic TestingDNA, FungalChromosomes, Human, Pair 22Chromosomes, Human, Pair 8Pregnancy OutcomeMyelodysplastic-Myeloproliferative DiseasesGestational AgeChromosomes, Human, Pair 11Chromosome MappingSyndromeChromosome BreakageNeoplasms, Adipose TissueChromosomes, Artificial, BacterialX ChromosomePloidiesChromosomes, Human, Pair 12Oligonucleotide Array Sequence AnalysisPhenotypeInfant, NewbornChromosomes, FungalSex Determination AnalysisGene DosageAmniotic FluidInfertility, MaleChromosomal InstabilityPreimplantation DiagnosisChromosomes, Human, Pair 3Polymerase Chain ReactionGenetic MarkersChromosomes, Human, 6-12 and XOligospermiaPrognosis