DeafnessHearing Loss, SensorineuralHearing LossCochleaPedigreeGenes, RecessiveEar, InnerEvoked Potentials, Auditory, Brain StemConnexinsSyndromeHearing Loss, UnilateralHair Cells, AuditoryStria VascularisSpiral GanglionHearingCochlear ImplantsHearing Loss, BilateralAudiometryConsanguinityCochlear ImplantationUsher SyndromesMutationLipreadingHearing TestsHearing Loss, CentralEndolymphWolfram SyndromeSign LanguageWaardenburg SyndromeCochlear NerveHypoparathyroidismAuditory ThresholdOrgan of CortiAudiometry, Pure-ToneHair Cells, Auditory, InnerJervell-Lange Nielsen SyndromeStereociliaDNA Mutational AnalysisCochlear DiseasesTectorial MembraneGenetic LinkageVestibular DiseasesStapesChromosome MappingMutation, MissenseTranscription Factor Brn-3CHearing DisordersAbnormalities, MultipleGenes, DominantPhenotypeKCNQ Potassium ChannelsVestibular AqueductHair ColorPersons With Hearing ImpairmentsHearing Loss, ConductiveLabyrinth DiseasesIchthyosisTemporal BoneCochlear DuctAtaxiaGoiterHair Cells, Auditory, OuterDNA, MitochondrialMolecular Sequence DataHearing AidsNephritis, HereditaryBulbar Palsy, ProgressiveVestibule, LabyrinthEarColobomaAcoustic StimulationKeratoderma, PalmoplantarPoint MutationAuditory CortexNational Institute on Deafness and Other Communication Disorders (U.S.)Genetic TestingLod ScoreHomozygoteCochlear Nucleus