Trinucleotide Repeat ExpansionTrinucleotide RepeatsFriedreich AtaxiaDNA Repeat ExpansionSpinocerebellar DegenerationsMyotonic DystrophyFragile X SyndromeRecombination, GeneticHuntington DiseaseFragile X Mental Retardation ProteinMicrosatellite RepeatsIron-Binding ProteinsAllelesRepetitive Sequences, Nucleic AcidBase SequenceMutationTandem Repeat SequencesMolecular Sequence DataSpinocerebellar AtaxiasDNAMachado-Joseph DiseaseGenetic MarkersPolymorphism, GeneticGenomic InstabilityHeredodegenerative Disorders, Nervous SystemGenetic VariationDNA, SatelliteMinisatellite RepeatsPolymerase Chain ReactionModels, GeneticNerve Tissue ProteinsSequence Analysis, DNADinucleotide RepeatsNucleic Acid ConformationPedigreeFlap EndonucleasesChromosome MappingFrontotemporal DementiaAnticipation, GeneticDNA RepairInverted Repeat SequencesGenotypeDNA PrimersCerebellar AtaxiaAge of OnsetEvolution, MolecularChromosome FragilityGenetic Diseases, InbornIntranuclear Inclusion BodiesAmino Acid SequenceHomologous RecombinationGenetic LinkagePhenotypeMuscular Dystrophy, OculopharyngealRNA-Binding ProteinsNuclear ProteinsHaplotypesDNA-Binding ProteinsGenetics, PopulationSaccharomyces cerevisiaeHeterozygotePhylogenyGene FrequencyDNA ReplicationGenome, HumanAmyotrophic Lateral SclerosisProteinsTranscription, GeneticPeptidesNeurodegenerative DiseasesCrossing Over, GeneticDNA, PlantDNA, FungalMice, TransgenicExonsCloning, MolecularRepetitive Sequences, Amino AcidNucleic Acid HeteroduplexesSaccharomyces cerevisiae ProteinsRad52 DNA Repair and Recombination ProteinGenes, DominantBlotting, SouthernMutS Homolog 2 ProteinSpecies SpecificityReceptors, AndrogenCell LineSequence Homology, Nucleic AcidV(D)J RecombinationPlasmidsRNA, MessengerSequence DeletionX ChromosomeMeiosisGenetic LociDNA Mutational AnalysisExpressed Sequence TagsGene ConversionChromosomes, Human, XEndodeoxyribonucleasesGenome