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Academic Journal

Is deafness etiology important for prediction of functional outcomes in pediatric cochlear implantation?

Subjects: GENETICS of deafness; ACADEMIC medical centers; AUDITORY perception testingSLOVAKIA

  • Source: Acta Oto-Laryngologica. Jun2014, Vol. 134 Issue 6, p571-578. 8p.

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Academic Journal

Systematic review of outcomes of cochlear implantation of different genotypes in patients with auditory neuropathy spectrum disorder.

Subjects: COCHLEAR implants; TREATMENT effectiveness; DESCRIPTIVE statistics

  • Source: Egyptian Journal of Otolaryngology; 9/17/2024, Vol. 40 Issue 1, p1-19, 19p

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Academic Journal

Targeted Exon Sequencing Successfully Discovers Rare Causative Genes and Clarifies the Molecular Epidemiology of Japanese Deafness Patients.

Subjects: DEAFNESS; EXONS (Genetics); NUCLEOTIDE sequence

  • Source: PLoS ONE; Aug2013, Vol. 8 Issue 8, p1-11, 11p

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Academic Journal

Mitochondrial 12s rRNA mutation A1555G: validation of a genotyping method.

Subjects: MITOCHONDRIA; RIBOSOMAL RNA; GENETIC mutation

  • Source: Minerva Biotechnology & Biomolecular Research; Jun2022, Vol. 34 Issue 2, p49-54, 6p

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Academic Journal

Occurrence of Del( GIB6 -D13S1830) Mutation in Italian Non-syndromic Hearing Loss Patients Carrying a Single GJB2 Mutated Allele.

Subjects: CONNEXINS; GENETIC mutation; HEARING disordersEUROPE

  • Source: Acta Oto-Laryngologica (Supplement). May2004 Supplement 552, Vol. 124, p29-34. 6p.

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Academic Journal

Recurrence of reported CDH23 mutations causing DFNB12 in a special cohort of South Indian hearing impaired assortative mating families – an evaluation.

Subjects: DEAFNESS; GENETIC mutation; EXOMES

  • Source: Annals of Human Genetics; Mar2018, Vol. 82 Issue 2, p119-126, 8p

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Academic Journal

MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin.

Subjects: GENETIC mutation; HEALTH impact assessment; NUCLEOTIDE sequence

  • Source: PLoS ONE; Apr2015, Vol. 10 Issue 4, p1-13, 13p

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Academic Journal

GJB2 and MTRNR1 contributions in children with hearing impairment from Northern Cameroon.

Subjects: HEARING impaired children; COMPUTER software; HEARING disordersSUB-Saharan Africa; CAMEROON

  • Source: International Journal of Audiology. Feb2011, Vol. 50 Issue 2, p133-138. 6p. 4 Charts.

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Academic Journal

Screening for GJB2 and GJB6 mutations in the Slovak deaf population.

Subjects: *GENETICS of deafness; *CONFERENCES & conventions; *GENESGERMANY; SLOVAKIA

  • Source: GMS Current Posters in Otorhinolaryngology: Head & Neck Surgery. 2013, Vol. 9, p1-1. 1p.

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  • 1-9 of  9 results for ""Deafness etiology""