DeafnessGeneticsHearing Loss, SensorineuralGenetics, PopulationHearing LossCochleaPedigreeGenes, RecessiveEar, InnerEvoked Potentials, Auditory, Brain StemSyndromeConnexinsMutationGenetics, BehavioralHearing Loss, UnilateralHair Cells, AuditoryPhenotypeStria VascularisSpiral GanglionGenetic LinkageHearingConsanguinityChromosome MappingCochlear ImplantsHearing Loss, BilateralAudiometryGenetic TestingCochlear ImplantationUsher SyndromesHearing TestsLipreadingHearing Loss, CentralEndolymphMolecular BiologyDNA Mutational AnalysisGenetic Predisposition to DiseaseWolfram SyndromeGenetic VariationSign LanguageWaardenburg SyndromeCochlear NerveGenetic CounselingHypoparathyroidismAuditory ThresholdOrgan of CortiAllelesAudiometry, Pure-ToneGenotypeMolecular Sequence DataHair Cells, Auditory, InnerGenes, DominantGenetic MarkersModels, GeneticMutation, MissenseJervell-Lange Nielsen SyndromeStereociliaDNA, MitochondrialCochlear DiseasesTectorial MembraneHair ColorVestibular DiseasesStapesHearing Loss, ConductiveAbnormalities, MultipleTranscription Factor Brn-3CHearing DisordersHeterozygoteLod ScoreHomozygoteKCNQ Potassium ChannelsVestibular AqueductPersons With Hearing ImpairmentsAtaxiaGenetic Diseases, InbornLabyrinth DiseasesBase SequenceIchthyosisTemporal BoneSequence Analysis, DNACochlear DuctHaplotypesGoiterMicrosatellite RepeatsHair Cells, Auditory, OuterPoint MutationPolymorphism, Single NucleotideGenetic ServicesHearing AidsNephritis, HereditaryBulbar Palsy, ProgressiveVestibule, LabyrinthGenetic ResearchEarGenome-Wide Association StudyColobomaFamily HealthAcoustic StimulationAmino Acid SequenceCrosses, GeneticDisease Models, Animal