Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Clinical implications of molecular genetic research in otorhinolaryngology].

Therapeutische Umschau. Revue therapeutique - 1 Aug 2003

Gürtler N

Abstract excerpt

Molecular-genetic research in Otolaryngology has seen a rapid advancement during the last ten years, especially in the fields of otology and head and neck tumors. The results of this basic research have now started to be implemented in the clinic. In otology the understanding of auditive function has dramatically improved. The syndromic and non-syndromic forms of hereditary hearing impairment can be subdivided...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Connexin 26
Share to Connexins
Share to Genetic Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Therapy

Share to Head and Neck Neoplasms

Share to Hearing Disorders

Share to Syndrome

Share to Wolfram Syndrome

Source

Identifiers

PMID: 14502856
DOI: 10.1024/0040-5930.60.8.477

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Clinical implications of molecular genetic research in otorhinolaryngology].PMID 14502856Read ↗

[Changes in the connexin 26 (GJB2) gene in Russian patients with hearing disorders: results of long-term molecular diagnostics of hereditary nonsyndromic deafness].Semantic proximity Read ↗

[Molecular biology and molecular genetics in the field of otorhinolaryngology--isolation of genes responsible for deafness].Semantic proximity Read ↗

[Congenital hearing loss. Molecular genetic diagnosis of connexin genes and genetic counselling].Semantic proximity Read ↗

[Molecular and functional testing in case of hereditary hearing loss associated with the SLC26A4 gene].Semantic proximity Read ↗

Connexin 26 mutations in nonsyndromic autosomal recessive hearing loss: speech and hearing rehabilitation.Semantic proximity Read ↗

[Personalized medicine in otology. The role of genetic diagnostics in patients with hearing impairment].Semantic proximity Read ↗

Functional Testing of SLC26A4 Variants-Clinical and Molecular Analysis of a Cohort with Enlarged Vestibular Aqueduct from Austria.Semantic proximity Read ↗

Molecular investigation in children candidates and submitted to cochlear implantation.Semantic proximity Read ↗

[Genetic aspects of congenital sensorineural hearing loss].Semantic proximity Read ↗

[The principles of molecular diagnosis of recessive forms of prelingual non-syndromic hearing loss].Semantic proximity Read ↗

[Hereditary hearing loss due to mutations in the connexin-26 gene].Semantic proximity Read ↗

[Genetic screening for hearing disorders in newborn infants in combination with audiological screening].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.