KaryotypingSpectral KaryotypingChromosome AberrationsChromosome DisordersKaryotypeIn Situ Hybridization, FluorescencePrenatal DiagnosisTrisomyAmniocentesisAneuploidyChromosome BandingCytogeneticsFetal DiseasesDown SyndromeCytogenetic AnalysisChorionic Villi SamplingSex Chromosome DisordersUltrasonography, PrenatalChromosome PaintingChromosomes, HumanComparative Genomic HybridizationAbnormal KaryotypePregnancyTranslocation, GeneticChromosomes, Human, Pair 18Ring ChromosomesChromosomes, Human, Pair 13NeckSex Chromosome AberrationsAbnormalities, MultipleAzure StainsChromosomes, Human, Pair 20Chromosome DeletionPregnancy Trimester, FirstNectriaChromosomes, Human, Pair 7Myelodysplastic-Myeloproliferative DiseasesPregnancy, High-RiskMetaphaseChromosomesCrown-Rump LengthUniparental DisomyMaternal AgeNuchal Translucency MeasurementMycological Typing TechniquesPregnancy Trimester, SecondAbortion, HabitualIntellectual DisabilityNucleic Acid HybridizationMosaicismNeoplasms, Adipose TissueAzoospermiaGenetic TestingChromosomes, Human, YSex Chromosome Disorders of Sex DevelopmentChromosomes, Human, Pair 5Gene RearrangementPregnancy OutcomeChromosomes, Human, XOligonucleotide Array Sequence AnalysisKlinefelter SyndromeChromosomes, Human, Pair 14Chromosomes, Human, Pair 21Gestational AgeDNA, 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 AmplificationPolymorphism, Single Nucleotide