PhenotypeConnexinsCataractConnexin 43MutationSyndactylyEye AbnormalitiesGenes, DominantPedigreeDNA Mutational AnalysisMolecular Sequence DataEye ProteinsTooth AbnormalitiesMutation, MissenseBase SequenceChromosomes, Human, Pair 13Gap JunctionsMicrophthalmosgamma-CrystallinsGenotypeGenetic LinkageAmino Acid SequenceLimb Deformities, CongenitalCraniofacial AbnormalitiesPelizaeus-Merzbacher DiseaseMice, Inbred C57BLLens, CrystallineChromosome MappingMice, KnockoutOdontodysplasiaAnterior Eye SegmentHeterozygoteAllelesCell DifferentiationLod ScoreFoot Deformities, CongenitalHaplotypesSequence Analysis, DNACells, CulturedAbnormalities, MultipleGenetic Complementation TestGenes, RecessiveMice, TransgenicGenetic Association StudiesGene DeletionSignal TransductionMicrosatellite RepeatsPolymerase Chain ReactionAmino Acid SubstitutionPoint MutationSyndromeAsian Continental Ancestry GroupTranscription FactorsRNA, MessengerFamilySequence AlignmentCell LineExonsImmunophenotypingLens Nucleus, CrystallineGenetic Predisposition to DiseaseCrosses, GeneticGene Expression Regulation, DevelopmentalDisease Models, AnimalPolymorphism, Single NucleotideHomozygoteGene ExpressionGene Expression RegulationChromosomes, Human, Pair 1Mutant ProteinsGenetic TestingBacterial ProteinsMembrane ProteinsCloning, MolecularGene Expression ProfilingImmunohistochemistryReverse Transcriptase Polymerase Chain ReactionDNA-Binding ProteinsParturitionCell DivisionIndiaalpha-CrystallinsMutagenesis, InsertionalModels, GeneticDrosophila ProteinsDNA PrimersMutagenesisCell ProliferationSaccharomyces cerevisiaeArabidopsisFlow CytometryGenetic VariationMice, Mutant StrainsSequence Homology, Amino AcidSuppression, GeneticArabidopsis ProteinsTranscription, GeneticGenes, LethalModels, BiologicalCell Transformation, Neoplastic