KaryotypingSpectral KaryotypingChromosome DisordersAmniocentesisDown SyndromeChorionic Villi SamplingNeckUltrasonography, PrenatalFetal DiseasesPregnancy Trimester, FirstPrenatal DiagnosisChromosome AberrationsPregnancy Trimester, SecondPregnancyPregnancy OutcomeGestational AgeKaryotypeIn Situ Hybridization, FluorescenceTrisomyAneuploidyChromosome BandingCytogeneticsCytogenetic AnalysisSex Chromosome DisordersChromosome PaintingChromosomes, HumanComparative Genomic HybridizationAbnormal KaryotypeTranslocation, GeneticChromosomes, Human, Pair 18Ring ChromosomesChromosomes, Human, Pair 13Sex Chromosome AberrationsAbnormalities, MultipleAzure StainsChromosomes, Human, Pair 20Chromosome DeletionNectriaChromosomes, Human, Pair 7Myelodysplastic-Myeloproliferative DiseasesPregnancy, High-RiskMetaphaseChromosomesCrown-Rump LengthUniparental DisomyMaternal AgeNuchal Translucency MeasurementMycological Typing TechniquesAbortion, HabitualIntellectual DisabilityNucleic Acid HybridizationMosaicismNeoplasms, Adipose TissueAzoospermiaGenetic TestingChromosomes, Human, YSex Chromosome Disorders of Sex DevelopmentChromosomes, Human, Pair 5Gene RearrangementChromosomes, Human, XOligonucleotide Array Sequence AnalysisKlinefelter SyndromeChromosomes, Human, Pair 14Chromosomes, Human, Pair 21DNA, FungalMonosomyChromosome BreakageAbortion, SpontaneousMyelodysplastic SyndromesCytoplasmic DyneinsChromosomes, Artificial, BacterialTurner SyndromeChromosomes, Human, Pair 8Sex Determination AnalysisPulmonary AtresiaGene DosageSyndromeChromosomal InstabilityPreimplantation DiagnosisAmniotic FluidChromosomes, Human, Pair 22DNA Copy Number VariationsInfertilityPolymerase Chain ReactionInfant, NewbornChromosome InversionChromosomes, Human, Pair 12Chromosomes, FungalFetusGenome, HumanCandidiasisInfertility, MaleChromosomes, Human, Pair 11Chromosome MappingDiploidyChromosomes, Human, Pair 3CandidaOligospermiaGene Amplification