Dosage Compensation, GeneticX Chromosome InactivationX ChromosomeGenes, X-LinkedSex ChromosomesMammalsRNA, Long NoncodingRNA, UntranslatedChromosomes, Human, XSex Chromosome AberrationsGenomic ImprintingMolecular Sequence DataIncontinentia PigmentiIn Situ Hybridization, FluorescenceTurner SyndromeGene SilencingMosaicismHybrid CellsRing ChromosomesEmbryo, MammalianCell LineHeterozygoteChromosome MappingMutationAllelesBase SequenceEquidaeTwins, MonozygoticHistonesGenetic LinkageAmino Acid SequenceTranscription FactorsDNA MethylationPedigreeMethylationOrofaciodigital SyndromesRett SyndromeVirus InactivationKineticsKaryotypingPhenotypeChromosomes, MammalianArylsulfatasesStem CellsReceptors, AndrogenPolycomb-Group ProteinsLong Interspersed Nucleotide ElementsGene DeletionCells, CulturedTranscription, GeneticTransgenesSteryl-SulfataseIntellectual DisabilityRepressor ProteinsPolymerase Chain ReactionDNATripletsPelizaeus-Merzbacher DiseaseGene Expression Regulation, DevelopmentalGene Expression RegulationDAX-1 Orphan Nuclear ReceptorBlastocystGenetic Diseases, X-LinkedY ChromosomeMethyl-CpG-Binding Protein 2Genetic MarkersChromosomes, Artificial, YeastFibroblastsEpigenesis, GeneticEmbryonic and Fetal DevelopmentDNA-Binding ProteinsCpG IslandsHeterozygote DetectionTranslocation, GeneticLysineModels, GeneticOxidoreductases, N-DemethylatingChromatinMice, TransgenicPolycomb Repressive Complex 2Gene ExpressionRNA, MessengerSequence DeletionSequence Homology, Amino AcidDNA ProbesProteinsSpecies SpecificityDNA PrimersSodium ChannelsIon Channel GatingCloning, MolecularMice, Inbred C57BLProtein BindingPlacentaMembrane PotentialsBlotting, SouthernAcetylationBinding SitesSignal TransductionRecombinant Proteins