Preimplantation DiagnosisPredictive Value of TestsBlastomeresChromosome AberrationsSex PreselectionGenetic TestingIn Situ Hybridization, FluorescencePrenatal DiagnosisPregnancySensitivity and SpecificityMutationAneuploidyChromosome DisordersFertilization in VitroEmbryo TransferTranslocation, GeneticPolymerase Chain ReactionHeterozygote DetectionGenetic Diseases, InbornPedigreeHeterozygoteKaryotypingDNA Mutational AnalysisBiopsyCytogenetic AnalysisGenetic CounselingSex Determination AnalysisChromosomes, Human, Pair 13Reproductive Techniques, AssistedPrognosisPregnancy OutcomeChromosomes, HumanSperm Injections, IntracytoplasmicInfant, NewbornRetrospective StudiesReproducibility of ResultsBlastocystMolecular Diagnostic TechniquesFalse Positive ReactionsPhenotypeLoss of HeterozygosityEugenicsProspective StudiesAbnormal KaryotypeChromosomes, Human, Pair 14Comparative Genomic Hybridizationbeta-ThalassemiaInfertility, MaleChromosomes, Human, Pair 17OmanMicrosatellite RepeatsSex Chromosome AberrationsChromosomes, Human, Pair 18Genetic Predisposition to DiseaseTrisomyGenotypeROC CurveEarly DiagnosisChorionic Villi SamplingGenetic Diseases, X-LinkedExonsCleavage Stage, OvumChromosome DeletionCongenital AbnormalitiesPolymorphism, Single-Stranded ConformationalVitrificationGenetic MarkersHomozygoteChromosomes, Human, Pair 21Risk FactorsSurrogate MothersAllelesEmbryonic DevelopmentPregnancy RateDelayed DiagnosisTomography, X-Ray ComputedEmbryo ResearchChromosomes, Human, Pair 11Treatment OutcomeChromosomes, Human, Pair 3Tumor Markers, BiologicalGenes, p53Cohort StudiesEmbryo, MammalianMosaicismBase SequenceExomeKlinefelter SyndromeDisease ProgressionOncogene Proteins, FusionChromosomes, Human, Pair 9Magnetic Resonance ImagingFollow-Up StudiesFalse Negative ReactionsCystic FibrosisCryopreservationTime FactorsSyndromeNucleic Acid Amplification TechniquesImmunohistochemistry