about
Nonsyndromic hearing impairment is associated with a mutation in DFNA5Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing lossA truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing lossA missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) miceDFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23The Bjornstad syndrome (sensorineural hearing loss and pili torti) disease gene maps to chromosome 2q34-36Isolation from cochlea of a novel human intronless gene with predominant fetal expressionLinkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3Nonsyndromic hearing impairment: unparalleled heterogeneityA gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24The Genetics of Deafness in Domestic AnimalsGenetics of hearing and deafnessSLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueductRFX transcription factors are essential for hearing in mice.An automated microfluidic system for single-stranded DNA preparation and magnetic bead-based microarray analysis.The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani PopulationsAssociation between X-linked mixed deafness and mutations in the POU domain gene POU3F4Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probandsNovel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafnessGJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE reviewMutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairmentAssembly of the cochlear gap junction macromolecular complex requires connexin 26.Mice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing loss.A new mouse insertional mutation that causes sensorineural deafness and vestibular defectsInner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndromeRelevance of connexin deafness (DFNB1) to human evolution.Kata Kolok Color Terms and the Emergence of Lexical Signs in Rural Signing CommunitiesAssessment of hearing in 80 inbred strains of mice by ABR threshold analyses.Otoprotective effects of ethosuximide in NOD/LtJ mice with age-related hearing lossGene Therapy Restores Hair Cell Stereocilia Morphology in Inner Ears of Deaf Whirler Mice.Genetic characteristics of the couple with non-syndromic sensorineural hearing loss and fertility guidance.Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations.Inner ear cell therapy targeting hereditary deafness by activation of stem cell homing factorsThe use of neurotrophin therapy in the inner ear to augment cochlear implantation outcomes.Age-Related Hearing Impairment (ARHI) associated with GJB2 single mutation IVS1+1G>A in the Yakut population isolate in Eastern Siberia.Significance of heterozygosis M34T mutation of GJB2 gene in non-syndromic congenital deafness. Retrospective analysis of 12,472 samples of amniotic fluid.Advancing genetic testing for deafness with genomic technology.Genetics of hearing loss: focus on DFNA2.Identifying the genes of hearing, deafness, and dysequilibrium.
P2860
Q22003955-73B7D409-99AD-41D1-AFF0-B6317DF44E9EQ24300273-8BC5E907-4196-44FB-95E5-980A35C88768Q24310602-2E49EE8F-9B57-4D35-A032-5C874F064CB6Q24529109-842765A4-7459-436E-9D8C-71CF3AD56C6EQ24535597-2C34C952-4D48-4D40-9F68-043AFA7E28FDQ24535604-306C9F8C-687F-457D-9463-6DD8929748F2Q24538930-BAFAB757-5070-420E-87CE-76CFF53DADC8Q24650440-19773F57-151A-47E1-B93F-CFD76968D32EQ24675154-33CF0FDB-24B8-488B-91EC-1389CF3121B2Q24680416-170B4A72-EBAC-473F-BBD2-E09A17458FAFQ24680575-C372FDCF-3201-4AE9-A62D-D435AE01F5EBQ26776085-EA94570D-2DE4-432E-AD86-177FFE2357B4Q26865293-E3A84888-AFD5-4B33-904D-BDED8A46315DQ27010177-D6ABC83D-DFA2-41C9-88E0-8C3BBA75A6BEQ27321262-21531489-88E5-4FC2-B98D-62EC96F39E5FQ27331965-22626563-D91D-41F4-9541-4719C3327530Q28087697-E387F688-E8A2-424D-BCD2-8F15541B222CQ28119014-FC8F82B1-5997-46B7-98A9-B564A94F925FQ28187639-C13868DA-0850-48CE-984B-E784C745B612Q28207545-3D161315-EBE9-4E7B-9373-FB2151FD4034Q28217345-3E607DAB-5366-4C00-803C-C31AB625B224Q28290745-A0C2BF76-7B15-4B84-A7B1-27AD24A0B427Q28507910-929EAE3D-9151-45FE-8F06-13B63E0B51C7Q28590867-31B12020-349C-467D-A30E-C43D953F818EQ28591820-902D363E-0A69-455B-BF84-72A337A035DCQ28593604-050D9373-EDF1-4B82-858B-A5696FE2C033Q28769547-C3F07FBE-7AFC-40C5-84F8-3273403A765AQ29399927-8F276738-68E8-4834-AB38-ED9BC7AA41ABQ29619783-CE075D98-0D12-46B2-B95C-ADF20E40E75AQ30354158-F58C215F-4A4E-492F-8456-21A02487C1CAQ30364634-66A9A1D4-8FB7-414B-899D-DD4D93ED63EBQ30390935-DD30456C-9594-410C-B5CB-DAD0FDECD1A2Q30412441-C84C1C2A-34C2-4711-AB06-2238854E914FQ30418975-B838F51C-A778-4E0D-8C15-90330F659538Q30435375-09E2DE90-6477-450D-A718-E6E683DA98D9Q30435992-14DFF7C2-7C91-4652-A91B-C234CB3F30BEQ30441969-D893075E-A456-4031-90A3-27B588397746Q30444538-ABC72A0B-DB1E-4899-8AE9-39A277AB264DQ30453431-8DF55B49-34F9-42CB-9629-75EFE6990874Q30454214-7B3A67DF-EAE8-4302-BE14-B89D05D9F849
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
gotara zanistî
@ku-latn
scientific article published on January 1991
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
name
Genetic epidemiology of hearing impairment.
@en
Genetic epidemiology of hearing impairment.
@nl
type
label
Genetic epidemiology of hearing impairment.
@en
Genetic epidemiology of hearing impairment.
@nl
prefLabel
Genetic epidemiology of hearing impairment.
@en
Genetic epidemiology of hearing impairment.
@nl
P1476
Genetic epidemiology of hearing impairment.
@en
P2860
P356
10.1111/J.1749-6632.1991.TB19572.X
P407
P577
1991-01-01T00:00:00Z