Preimplantation DiagnosisPredictive Value of TestsBlastomeresSex PreselectionPrenatal DiagnosisGenetic TestingPregnancySensitivity and SpecificityFertilization in VitroEmbryo TransferHeterozygote DetectionGenetic Diseases, InbornIn Situ Hybridization, FluorescenceAneuploidyPolymerase Chain ReactionGenetic CounselingSex Determination AnalysisHeterozygoteReproductive Techniques, AssistedBiopsyMutationPregnancy OutcomeSperm Injections, IntracytoplasmicPedigreeChromosome DisordersMolecular Diagnostic TechniquesReproducibility of ResultsRetrospective StudiesBlastocystFalse Positive ReactionsProspective StudiesEugenicsChromosome AberrationsPrimary Preventionbeta-ThalassemiaTranslocation, GeneticDNA Mutational AnalysisInfant, NewbornEarly DiagnosisROC CurveChorionic Villi SamplingCleavage Stage, OvumGenetic Diseases, X-LinkedRisk FactorsVitrificationSurrogate MothersPregnancy RateDelayed DiagnosisPrognosisEmbryo ResearchChromosomes, Human, Pair 21Embryonic DevelopmentCohort StudiesExomeFollow-Up StudiesChromosomes, Human, Pair 13Tomography, X-Ray ComputedTime FactorsEmbryo, MammalianGenotypeChromosomes, HumanTreatment OutcomeCryopreservationCystic FibrosisNucleic Acid Amplification TechniquesKaryotypingMosaicismKlinefelter SyndromeFalse Negative ReactionsCytogenetic AnalysisHistocompatibility TestingMyotonic DystrophyConsanguinityMitochondrial DiseasesCenters for Disease Control and Prevention (U.S.)Embryo DispositionSecondary PreventionMicrosatellite RepeatsMitochondrial Trifunctional Protein, alpha SubunitDiagnostic ErrorsDiagnosisBiological MarkersExonsAbortion, HabitualEmbryo ImplantationMass ScreeningGenetic Predisposition to DiseaseReproductive TechniquesInfertilityKaryotypeEthics, MedicalRisk AssessmentAllelesGenetic MarkersUnited StatesInfertility, MaleEmbryo Culture TechniquesIncidenceGenetic LinkagePrevalence