Trinucleotide Repeat ExpansionTrinucleotide RepeatsMyotonic DystrophyFriedreich AtaxiaDNA Repeat ExpansionSpinocerebellar DegenerationsFragile X SyndromeHuntington DiseaseFragile X Mental Retardation ProteinMicrosatellite RepeatsIron-Binding ProteinsAllelesRNA-Binding ProteinsChromosome MappingChromosomesMutationRepetitive Sequences, Nucleic AcidBase SequenceNuclear ProteinsMolecular Sequence DataSpinocerebellar AtaxiasAlternative SplicingMachado-Joseph DiseaseGenetic MarkersX ChromosomeDrosophila ProteinsHeredodegenerative Disorders, Nervous SystemDNAPedigreePolymorphism, GeneticGenomic InstabilityNerve Tissue ProteinsDinucleotide RepeatsPolymerase Chain ReactionTroponin TMinisatellite RepeatsTandem Repeat SequencesFrontotemporal DementiaDrosophilaFlap EndonucleasesChromosome BandingDNA, SatelliteGenetic VariationAnticipation, GeneticNucleic Acid ConformationChromosome FragilitySequence Analysis, DNAGenetic LinkageInverted Repeat SequencesChromosomes, Human, Pair 9Sex ChromosomesGenotypeAge of OnsetChromosomes, Human, XChromosome AberrationsModels, GeneticCerebellar AtaxiaChromosomes, Human, Pair 1PhenotypeChromosomes, HumanIntranuclear Inclusion BodiesGenetic Diseases, InbornMuscular Dystrophy, OculopharyngealHaplotypesDNA PrimersHeterozygoteChromosome SegregationChromosomes, BacterialGenome, HumanGene FrequencyChromosomes, Human, Pair 6Chromosomes, PlantChromosome DeletionChromosomes, Human, Pair 7Amyotrophic Lateral SclerosisChromosomes, Human, Pair 11Genetics, PopulationChromosomes, Human, Pair 17Chromosomes, Human, YRecombination, GeneticChromosomes, MammalianNeurodegenerative DiseasesChromosomes, Artificial, BacterialProteinsEvolution, MolecularDNA RepairChromosomes, Human, Pair 21Chromosomes, FungalDNA ReplicationChromosomes, Human, Pair 13Chromosomes, Human, Pair 2Genes, DominantPeptidesChromosomes, Human, 6-12 and XDNA, PlantChromosomes, Human, Pair 10Amino Acid SequenceSaccharomyces cerevisiaeExonsChromosomes, Human, Pair 16