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

[Gene mapping of a nonsyndromic hearing impairmint family].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Apr 2003

Cheng Lin, Gong Yaoqin, Liu Qiji, Chen Bingxi, Guo Chenhong, Li Jiangxia, Zhang Xiyu, Lu Yong, Gao Guimin, Zhou Haibin, Guo Yishou

Abstract excerpt

OBJECTIVE: To map the gene responsible for nonsyndromic hearing impairment in a consanguineous family. METHODS: Firstly, X chromosome scanning was used to exclude X chromosome. Secondly, candidate gene analyzing and genome scanning were performed by homozygosity mapping. Then, additional markers...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 17
Share to Chromosomes, Human, Pair 18

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, X

Share to Consanguinity

Share to Family Health

Share to Hearing Loss, Sensorineural

Share to Microsatellite Repeats

Source

Identifiers

PMID: 12673573

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-12673573-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Gene mapping of a nonsyndromic hearing impairmint family].PMID 12673573Read ↗

[Genetic and audiological characters of a Chinese family with non-syndromic hereditary hearing loss].Semantic proximity Read ↗

[A family with nonsyndromic hearing impairment caused by intermarry].Semantic proximity Read ↗

[Study on mutations in the connexin 26 gene among Chinese with nonsyndromic hearing loss].Semantic proximity Read ↗

Linkage and association studies in a Malaysian family with autosomal recessive non-syndromic hearing loss.Semantic proximity Read ↗

Phenotype and genotype analysis of a Chinese family with prelingual X-linked hereditary hearing impairment.Semantic proximity Read ↗

Genome-wide SNP-based linkage analysis for ADNSHL families identifies novel susceptibility loci with positive evidence for linkage.Semantic proximity Read ↗

[Molecular analysis of the heterogeneity of hereditary monosymptomatic sensorineural hearing loss].Semantic proximity Read ↗

[c.359T>C mutation of the MYH14 gene in two autosomal dominant non-syndromic hearing impairment families with common ancestor].Semantic proximity Read ↗

[Association between nonsyndromic cleft lip/palate and microsatellite markers located in 4q].Semantic proximity Read ↗

Genomewide linkage analysis to presbycusis in the Framingham Heart Study.Semantic proximity Read ↗

[Mutation screening of 20 candidate genes located in chromo-some 5q31-5q32 for DFNA52 locus].Semantic proximity Read ↗

[A new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter].Semantic proximity Read ↗

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