KaryotypingSpectral KaryotypingChromosome AberrationsChromosome DisordersKaryotypeIn Situ Hybridization, FluorescencePrenatal DiagnosisTrisomyAmniocentesisAneuploidyChromosome BandingCytogeneticsFetal DiseasesDown SyndromeCytogenetic AnalysisChorionic Villi SamplingSex Chromosome DisordersUltrasonography, PrenatalChromosome PaintingChromosomes, HumanPregnancyComparative Genomic HybridizationAbnormal KaryotypeTranslocation, 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 TissueGenetic TestingAzoospermiaChromosomes, Human, YSex Chromosome Disorders of Sex DevelopmentChromosomes, Human, Pair 5Oligonucleotide Array Sequence AnalysisGene RearrangementPregnancy OutcomeChromosomes, Human, XKlinefelter SyndromeChromosomes, Human, Pair 14Chromosomes, Human, Pair 21Gestational AgeDNA, FungalMonosomyChromosome BreakageAbortion, SpontaneousMyelodysplastic SyndromesCytoplasmic DyneinsChromosomes, Artificial, BacterialSyndromeTurner SyndromeChromosomes, Human, Pair 8Sex Determination AnalysisPulmonary AtresiaGene DosageChromosomal InstabilityInfant, NewbornPreimplantation DiagnosisPolymerase Chain ReactionAmniotic FluidChromosomes, Human, Pair 22DNA Copy Number VariationsInfertilityGenome, HumanChromosome InversionChromosomes, Human, Pair 12Chromosome MappingChromosomes, FungalFetusPhenotypeCandidiasisInfertility, MaleChromosomes, Human, Pair 11Polymorphism, Single NucleotideDiploidySensitivity and SpecificityChromosomes, Human, Pair 3Candida