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Article

[Prenatal screening and diagnosis of genetic deafness by microarray].

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery - 1 Dec 2012

Sun Lian-hua, Li Lei, Wang Xiao-wen, Zhu Ya-zhong, Chai Yong-chuan, Li Xiao-hua, Wu Hao, Yang Tao

Abstract excerpt

OBJECTIVE: To evaluate a microarray-based mutation screening method for genetic deafness and its application in prenatal diagnosis. METHODS: Mutation screening of common deafness genes was performed in pregnant women and volunteers spouses. Nine common mutations in four major deafness genes, GJB2, GJB3, SLC26A4 and mitochondrial 12S rRNA, were detected simultaneously by a microarray-based method. Genetic...

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Source

Identifiers

PMID: 23328038

Genes

GJB2
GJB3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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