KaryotypingSpectral KaryotypingChromosome AberrationsChromosome DisordersKaryotypeIn Situ Hybridization, FluorescencePrenatal DiagnosisTrisomyAmniocentesisAneuploidyChromosome BandingCytogeneticsFetal DiseasesDown SyndromeCytogenetic AnalysisChorionic Villi SamplingSex Chromosome DisordersUltrasonography, PrenatalChromosome PaintingChromosomes, HumanComparative Genomic HybridizationPregnancyAbnormal KaryotypeTranslocation, GeneticChromosomes, Human, Pair 18Ring ChromosomesChromosomes, Human, Pair 13NeckSex Chromosome AberrationsAzure StainsAbnormalities, MultipleChromosomes, Human, Pair 20Chromosome DeletionPregnancy Trimester, FirstNectriaChromosomesChromosomes, Human, Pair 7Myelodysplastic-Myeloproliferative DiseasesPregnancy, High-RiskMetaphaseNucleic Acid HybridizationCrown-Rump LengthUniparental DisomyMycological Typing TechniquesMaternal AgeNuchal Translucency MeasurementPregnancy Trimester, SecondAbortion, HabitualIntellectual DisabilityMolecular Sequence DataMosaicismOligonucleotide Array Sequence AnalysisNeoplasms, Adipose TissueGenetic TestingDNA, FungalAzoospermiaChromosomes, Human, YSequence Analysis, DNAGene RearrangementPolymerase Chain ReactionSex Chromosome Disorders of Sex DevelopmentChromosomes, Human, Pair 5Pregnancy OutcomeChromosomes, Human, XChromosomes, Human, Pair 21PhenotypeKlinefelter SyndromeChromosomes, Human, Pair 14Gestational AgeChromosome BreakageMonosomyPhylogenyBacteriaChromosomes, Artificial, BacterialAbortion, SpontaneousGene DosageCytoplasmic DyneinsMyelodysplastic SyndromesTurner SyndromeSex Determination AnalysisChromosomes, Human, Pair 8Chromosome MappingSyndromePulmonary AtresiaBase SequenceChromosomal InstabilityInfant, NewbornCandidaCandidiasisAmniotic FluidPreimplantation DiagnosisMutationChromosomes, Human, Pair 22Chromosomes, FungalDNA Copy Number VariationsGenome, HumanGenomicsInfertilitySensitivity and SpecificityAquatic Organisms