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Article

Diagnosis routine and approach in genetic sensorineural hearing loss.

Brazilian journal of otorhinolaryngology - 1 Jan 2000

Abreu Alves Fatima Regina, Quintanilha Ribeiro Fernando de Andrade

Abstract excerpt

AIM: To develop a screening in order to determine the more common syndromic and non-syndromic genetic SNHL, considering epidemiological data, information and the development of new technologies; clinical implications and bioethical issues. MATERIALS AND METHODS: We reviewed the literature in order to develop a screening that includes: history, patterns of inheritance, physical evaluation, laboratory tests, image...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 17684664
DOI: 10.1016/s1808-8694(15)30087-2
PMCID: PMC9445739

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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