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Article

Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysis.

Molecular medicine reports - 1 Mar 2016

Ma Dingyuan, Zhang Jingjing, Luo Chunyu, Lin Ying, Ji Xiuqing, Hu Ping, Xu Zhengfeng

Abstract excerpt

The aim of the present study was to investigate the genetic etiology of patients with nonsyndromic hearing impairment through gene analysis, and provide accurate genetic counseling and prenatal diagnosis for deaf patients and families with deaf children. Previous molecular etiological studies have demonstrated that the most common molecular changes in Chinese patients with nonsyndromic hearing loss (NSHL)...

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Source

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Identifiers

PMID: 26783197
DOI: 10.3892/mmr.2016.4769
PMCID: PMC4769003

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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