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Preimplantation DiagnosisPredictive Value of TestsBlastomeresSex PreselectionEmbryo, MammalianPrenatal DiagnosisPregnancyGenetic TestingFertilization in VitroSensitivity and SpecificityEmbryo, NonmammalianBlastocystChick EmbryoEmbryo TransferEmbryo ImplantationHeterozygote DetectionIn Situ Hybridization, FluorescenceGenetic Diseases, InbornAneuploidyEmbryonic DevelopmentPolymerase Chain ReactionCleavage Stage, OvumSperm Injections, IntracytoplasmicSex Determination AnalysisMutationHeterozygotePregnancy OutcomeGenetic CounselingBiopsyReproductive Techniques, AssistedChromosome DisordersPedigreeEmbryo ResearchMolecular Diagnostic TechniquesReproducibility of ResultsPregnancy RateRetrospective StudiesEmbryo DispositionCryopreservationChromosome AberrationsFalse Positive ReactionsEugenicsVitrificationbeta-ThalassemiaTranslocation, GeneticDNA Mutational AnalysisProspective StudiesROC CurveEarly DiagnosisChorionic Villi SamplingGenetic Diseases, X-LinkedSurrogate MothersInfant, NewbornOocytesEmbryo LossChromosomes, Human, Pair 21Delayed DiagnosisMosaicismEmbryonic and Fetal DevelopmentGene Expression Regulation, DevelopmentalTime FactorsPrognosisReproductive TechniquesExomeGenotypeChromosomes, Human, Pair 13Chromosomes, HumanKaryotypingInfertilityCohort StudiesPhenotypeCytogenetic AnalysisTomography, X-Ray ComputedNucleic Acid Amplification TechniquesCystic FibrosisKlinefelter SyndromeFalse Negative ReactionsExonsAllelesBase SequenceMyotonic DystrophyHistocompatibility TestingMicrosatellite RepeatsAbortion, HabitualMitochondrial DiseasesConsanguinityBiological MarkersMitochondrial Trifunctional Protein, alpha SubunitKaryotypeDiagnosisMolecular Sequence DataDiagnostic ErrorsGenetic MarkersInfertility, MaleFollow-Up StudiesEthics, MedicalPregnancy Reduction, MultifetalSpermatozoaRisk FactorsGenetic Predisposition to Disease