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Concurrent Genetic and Standard Screening for Hearing Impairment in 9317 Southern Chinese Newborns.

Genetic testing and molecular biomarkers - 1 Oct 2016

Peng Qi, Huang Suran, Liang Yuan, Ma Keze, Li Siping, Yang Lin, Li Wenrui, Ma Qiang, Liu Qian, Zhong Baimao, Lu Xiaomei

Abstract excerpt

OBJECTIVE: The goal of this study was to investigate the use of concurrent genetic screening together with standard newborn hearing screening (NHS) in an effort to provide a scientific basis for the beneficial use of concurrent genetic hearing screening in newborns. Our aim was to improve the neonatal detection rate of hearing impairment and the potential for hearing loss, allowing for increased early...

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Identifiers

PMID: 27541434
DOI: 10.1089/gtmb.2016.0055

Genes

NHS
GJB2
GJB3

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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.

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