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

[Analysis of genotypes and hearing phenotypes of mutation infants with deafness].

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery - 1 Feb 2020

Wang Xianlei, Zhao Xuelei, Huang Lihui, Wen Cheng, Wang Xueyao, Cheng Xiaohua

Abstract excerpt

Objective:The aim of this study is to explore the genotype and hearing phenotype of deaf infants with mutation of GJB2 gene. Method:Subjects were 121 infants with GJB2 gene mutations who were treated in the Children's Hearing Diagnosis Center of Beijing Tongren hospital. All subjects were accepted to undertake the universal newborns hearing screening（UNHS） and series of objective audiometry, including auditory...

Read the complete abstract on PubMed

Topics

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

Share to Connexin 26
Share to Connexins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Deafness

Share to DNA Mutational Analysis

Share to Genotype

Share to Infant

Share to Infant, Newborn

Share to Phenotype

Source

Open in PubMed Open full text

Identifiers

PMID: 32086913
DOI: 10.13201/j.issn.1001-1781.2020.02.004
PMCID: PMC10128414

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Analysis of genotypes and hearing phenotypes of mutation infants with deafness].PMID 32086913Read ↗

[The effects of newborn genetic screening for GJB2 and hearing follow-ups].Semantic proximity Read ↗

[Analysis of genotype-phenotype correlation for GJB2 in 221 non-syndromic deafness probands and their pedigrees].Semantic proximity Read ↗

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

[Mutations of GJB2 gene in infants with non-syndromic hearing impairment].Semantic proximity Read ↗

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

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

[Clinical hearing phenotypes analysis of GJB2 gene p.V37I homozygote and compound heterozygote mutation in infants].Semantic proximity Read ↗

[The sequencing analyze of 915 newborn with GJB2 heterozygous mutation in Beijing].Semantic proximity Read ↗

[Genotype and clinical phenotype analysis of 42 patients with delayed nonsyndromic hearing loss].Semantic proximity Read ↗

[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype].Semantic proximity Read ↗

GJB2 gene mutations in newborns with non-syndromic hearing impairment in Northern China.Semantic proximity Read ↗

[Analysis on trend of hearing changes in infants with p.V37I mutation in GJB2 gene at different months of age].Semantic proximity Read ↗

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