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

[External quality survey results of newborn deafness gene mutations in China].

Zhonghua yi xue za zhi - 27 Jan 2015

Wang Wei, Zhong Kun, He Falin, Zhang Yan, Zhao Yan, Wang Zhiguo

Abstract excerpt

OBJECTIVE: To evaluate the external quality survey results of newborn hereditary deafness gene mutations to improve and enhance the testing quality of hereditary deafness gene mutations. METHODS: Each of 30 voluntarily participating laboratories testing newborn hereditary deafness gene mutations received 15 lots of quality control blood spots in this survey at May 2013, including mitochondria DNA 12SrRNA 1555A>G...

Read the complete abstract on PubMed

Topics

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

Share to China
Share to Connexin 26
Share to Connexins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Deafness

Share to DNA, Mitochondrial

Share to DNA Mutational Analysis

Share to Genetic Testing

Share to Infant, Newborn

Source

Identifiers

PMID: 25877242

Genes

GJB2

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

[External quality survey results of newborn deafness gene mutations in China].PMID 25877242Read ↗

[Current status of newborn deafness gene screeningin parts of China].Semantic proximity Read ↗

Clinical data analysis of genotypes and phenotypes of deafness gene mutations in newborns: A retrospective study.Semantic proximity Read ↗

Integrating Newborn Genetic Screening with Traditional Screening to Improve Newborn ScreeningSemantic proximity Read ↗

[A follow-up study of abnormal mutation in neonatal deafness gene screening].Semantic proximity Read ↗

[Analysis of the deafness gene screening results from newborns in Shijiazhuang].Semantic proximity Read ↗

[An analysis of the mutation in GJB2，GJB3，SLC26A4 and mtDNA12SrRNA in new born].Semantic proximity Read ↗

Genetic screening of newborns for deafness over 11 years in Beijing, China: More infants could benefit from an expanded program.Semantic proximity Read ↗

[Analysis of common mutations of deafness-related genes in 2725 newborns].Semantic proximity Read ↗

[Hearing assessment and follow-up study of aeonatal deafness gene screening homozygous mutation infants].Semantic proximity Read ↗

Concurrent Hearing and Genetic Screening of 18 001 Neonates with Hearing Diagnose in Nantong, ChinaSemantic proximity Read ↗

Newborn Screening of Genetic Mutations in Common Deafness Genes With Bloodspot-Based Gene Chip Array.Semantic proximity Read ↗

Concurrent Hearing and Genetic Screening among Newborns in Ningbo, China.Semantic proximity Read ↗

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