(Q28217345)

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

The cellular basis of hearing: the biophysics of hair cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Epidemiologic patterns in childhood hearing loss: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Genetic epidemiology of hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Mitochondrial defects and hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Connexin 26 gene linked to a dominant deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Relation between choice of partner and high frequency of connexin-26 deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations--molecular and audiological findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Sensorineural hearing loss and the incidence of Cx26 mutations in Austria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Molecular genetics applied to clinical practice: the Cx26 hearing impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Pattern of connexin 26 (GJB2) mutations causing sensorineural hearing impairment in Ghana

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

High carrier frequency of the 35delG deafness mutation in European populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Meta-analysis of GJB2 mutation 35delG frequencies in Europe

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Prevalence and characteristics of children with serious hearing impairment in metropolitan Atlanta, 1991-1993.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Connexin 26 studies in patients with sensorineural hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Prevalent connexin 26 gene (GJB2) mutations in Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Connexin26 mutations associated with nonsyndromic hearing loss.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Connexin 26 Gene Mutations in Congenitally Deaf Children

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

High frequency hearing loss correlated with mutations in the GJB2 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Connexin-26 gene analysis in hearing-impaired newborns.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Connexin-26 mutations in sporadic and inherited sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

The M34T allele variant of connexin 26.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350)

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

The effects of a connexin 26 mutation--35delG--on oto-acoustic emissions and brainstem evoked potentials: homozygotes and carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Year 2000 Position Statement: Principles and Guidelines for Early Hearing Detection and Intervention Programs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Attitudes of deaf adults toward genetic testing for hereditary deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Parental attitudes toward genetic testing for pediatric deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Determination of the frequency of the 35delG allele in Brazilian neonates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Nonradioactive detection of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi Jews

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Rapid detection of Campylobacter fetus by polymerase chain reaction combined with non-radioactive hybridization using an oligonucleotide covalently bound to microwells

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Rapid detection of the 35delG mutation in the GJB2 gene in childhood deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

GJB2 gene mutations in childhood deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004

Gap Junction Systems in the Rat Vestibular Labyrinth: Immunohistochemical and Ultrastructural Analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200207000-00004