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

A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3.

American journal of medical genetics. Part A - 15 Feb 2005

Aslam Muhammad, Wajid Muhammad, Chahrour Maria H, Ansar Muhammad, Haque Sayedul, Pham Thanh L, Santos Regie P, Yan Kai, Ahmad Wasim, Leal Suzanne M

Abstract excerpt

A consanguineous family with autosomal recessive nonsyndromic hearing impairment (NSHI) was ascertained in Pakistan and displayed significant evidence of linkage to 3q13.31-q22.3. The novel locus (DFNB42) segregating in this kindred, maps to a 21.6 cM region according to a genetic map constructed using data from both the deCode and Marshfield genetic maps. This region of homozygosity is flanked by markers D3S1278...

Read the complete abstract on PubMed

Topics

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

Share to Audiometry
Share to Chromosome Mapping

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 3

Share to Genes, Recessive

Share to Genetic Linkage

Share to Hearing Loss

Share to Lod Score

Share to Microsatellite Repeats

Source

Open in PubMed Open full text

Identifiers

PMID: 15641023
DOI: 10.1002/ajmg.a.30508
PMCID: PMC2909096

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3.PMID 15641023Read ↗

Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2.Semantic proximity Read ↗

DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.Semantic proximity Read ↗

A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4.Semantic proximity Read ↗

Mapping of a novel autosomal recessive nonsyndromic deafness locus (DFNB46) to chromosome 18p11.32-p11.31.Semantic proximity Read ↗

DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2.Semantic proximity Read ↗

Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3.Semantic proximity Read ↗

Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decades.Semantic proximity Read ↗

Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12.Semantic proximity Read ↗

A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9.Semantic proximity Read ↗

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.Semantic proximity Read ↗

Biallelic mutations in pakistani families with autosomal recessive prelingual nonsyndromic hearing loss.Semantic proximity Read ↗

Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani familiesSemantic proximity Read ↗

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