Pages that link to "Q37269361"
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The following pages link to Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients (Q37269361):
Displaying 31 items.
- Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing (Q21261480) (← links)
- Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis (Q26774741) (← links)
- GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss (Q28547852) (← links)
- Molecular screening of patients with nonsyndromic hearing loss from Nanjing city of China (Q28703821) (← links)
- Hereditary palmoplantar keratoderma and deafness resulting from genetic mutation of Connexin 26 (Q34159800) (← links)
- Efficient molecular genetic diagnosis of enlarged vestibular aqueducts in East Asians. (Q34190912) (← links)
- The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations (Q34221098) (← links)
- Exploration of molecular genetic etiology for Korean cochlear implantees with severe to profound hearing loss and its implication (Q34568122) (← links)
- A rapid method for simultaneous screening of multi-gene mutations associated with hearing loss in the Korean population (Q34613043) (← links)
- Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China. (Q34779797) (← links)
- Functional evaluation of GJB2 variants in nonsyndromic hearing loss. (Q35016960) (← links)
- A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family (Q35204053) (← links)
- Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China (Q35739700) (← links)
- Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans (Q35900790) (← links)
- A systematic review and meta-analysis of 235delC mutation of GJB2 gene (Q36235919) (← links)
- Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families (Q36392283) (← links)
- Construction of a DNA chip for screening of genetic hearing loss (Q37165767) (← links)
- A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family (Q37496120) (← links)
- A Novel Frameshift Mutation of SLC26A4 in a Korean Family With Nonsyndromic Hearing Loss and Enlarged Vestibular Aqueduct (Q37668389) (← links)
- Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations (Q37782545) (← links)
- GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype (Q38125413) (← links)
- Long Term Speech Perception Outcomes of Cochlear Implantation in Gap Junction Protein Beta 2 Related Hearing Loss. (Q41056371) (← links)
- Associations between GJB2, mitochondrial 12S rRNA, SLC26A4 mutations, and hearing loss among three ethnicities (Q41232716) (← links)
- Phenotype–Genotype Correlation in 295 Chinese Deaf Subjects with Biallelic Causative Mutations in the GJB2 Gene (Q44999132) (← links)
- Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China. (Q48275976) (← links)
- GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China (Q50316694) (← links)
- Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss (Q50354318) (← links)
- Prevalence of GJB6 mutations in Chinese patients with non-syndromic hearing loss (Q50432162) (← links)
- A Novel GJB2 compound heterozygous mutation c.257C>G (p.T86R)/c.176del16 (p.G59A fs*18) causes sensorineural hearing loss in a Chinese family. (Q52582883) (← links)
- Genetics of hereditary hearing loss in east Iran population: A systematic review of GJB2 mutations (Q90116929) (← links)
- Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations (Q90380905) (← links)