Preimplantation DiagnosisPredictive Value of TestsBlastomeresSex PreselectionPrenatal DiagnosisGenetic TestingSensitivity and SpecificityPregnancyFertilization in VitroEmbryo TransferHeterozygote DetectionGenetic Diseases, InbornIn Situ Hybridization, FluorescenceAneuploidyPolymerase Chain ReactionSex Determination AnalysisGenetic CounselingReproductive Techniques, AssistedHeterozygoteBiopsyMutationPregnancy OutcomeSperm Injections, IntracytoplasmicChromosome DisordersPedigreeMolecular Diagnostic TechniquesBlastocystReproducibility of ResultsFalse Positive ReactionsRetrospective StudiesEugenicsChromosome Aberrationsbeta-ThalassemiaTranslocation, GeneticDNA Mutational AnalysisProspective StudiesROC CurveEarly DiagnosisChorionic Villi SamplingCleavage Stage, OvumGenetic Diseases, X-LinkedVitrificationInfant, NewbornSurrogate MothersPregnancy RateDelayed DiagnosisEmbryo ResearchChromosomes, Human, Pair 21Embryonic DevelopmentPrognosisExomeChromosomes, Human, Pair 13Embryo, MammalianChromosomes, HumanTomography, X-Ray ComputedCohort StudiesCryopreservationCystic FibrosisNucleic Acid Amplification TechniquesKaryotypingMosaicismKlinefelter SyndromeGenotypeCytogenetic AnalysisFalse Negative ReactionsHistocompatibility TestingMyotonic DystrophyConsanguinityEmbryo DispositionMitochondrial Trifunctional Protein, alpha SubunitMicrosatellite RepeatsMitochondrial DiseasesDiagnosisExonsDiagnostic ErrorsAbortion, HabitualEmbryo ImplantationFollow-Up StudiesKaryotypeReproductive TechniquesInfertilityTime FactorsEthics, MedicalBiological MarkersGenetic MarkersAllelesRisk FactorsGenetic Predisposition to DiseaseInfertility, MaleEmbryo Culture TechniquesTreatment OutcomeGenetic LinkageReagent Kits, DiagnosticPregnancy Reduction, MultifetalSex Determination ProcessesSyndromePhenotypeMutation, MissenseLymphocytesDiagnosis, Computer-Assisted