A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
about
DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.Nonsyndromic hearing impairment: unparalleled heterogeneityA gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus.Genetics of Tinnitus: Still in its Infancy.A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.Auditory hair cell defects as potential cause for sensorineural deafness in Wolf-Hirschhorn syndromeTwo families with phenotypically different hereditary low frequency hearing impairment: longitudinal data and linkage analysis.A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findingsAutosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1Beginning of a molecular era in hearing and deafness.Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes.Whole-exome sequencing to decipher the genetic heterogeneity of hearing loss in a Chinese family with deaf by deaf mating.Human sequences homologous to the gene for the cochlear protein Ocp-II do not map to currently known non-syndromic hearing loss loci.Bilateral sensorineural deafness and hydrocephalus due to foramen of Monro obstruction in sibs: a newly described autosomal recessive disorder.Non-syndromic autosomal-dominant deafness.A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.Mutations in the Wolfram syndrome type 1 gene (WFS1) define a clinical entity of dominant low-frequency sensorineural hearing loss.WFS1 and GJB2 mutations in patients with bilateral low-frequency sensorineural hearing loss.[Phenotypic characterization of a DFNA6 family with low-frequency hearing loss].Further evidence for linkage of low-mid frequency hearing impairment to the candidate region on chromosome 4p16.3.
P2860
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P2860
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
description
1995 nî lūn-bûn
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1995 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
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1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
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name
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
@ast
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
@en
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
@nl
type
label
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
@ast
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
@en
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
@nl
prefLabel
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
@ast
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
@en
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
@nl
P2093
P356
P1476
A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3
@en
P2093
K Fukushima
M M Lesperance
T B San Agustin
P304
P356
10.1093/HMG/4.10.1967
P407
P577
1995-10-01T00:00:00Z