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

Infrequency of two deletion mutations at the DFNB1 locus in patients and controls.

American journal of medical genetics. Part A - 1 Apr 2008

Tang Hsiao-Yuan, Basehore Monica J, Blakey Gregory L, Darilek Sandra, Oghalai John S, Roa Benjamin B, Fang Ping, Alford Raye Lynn

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Base Sequence
Share to Case-Control Studies
Share to Connexin 26
Share to Connexins

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

Share to DNA Primers

Share to Genotype

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 18324688
DOI: 10.1002/ajmg.a.32207
PMCID: PMC3597119

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 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

Infrequency of two deletion mutations at the DFNB1 locus in patients and controls.PMID 18324688Read ↗

Clinical presentation of DFNB1.Semantic proximity Read ↗

Non-syndromic dominant DFNA1.Semantic proximity Read ↗

The clinical presentation of DFNB2.Semantic proximity Read ↗

Clinical presentation of the DFNA loci where causative genes have not yet been cloned. DFNA4, DFNA6/14, DFNA7, DFNA16, DFNA20 and DFNA21.Semantic proximity Read ↗

Clinical features of DFNA5.Semantic proximity Read ↗

A novel de novo pathogenic mutation in the CACNA1A gene.Semantic proximity Read ↗

Bi-allelic FRA10AC1 variants in a multisystem human syndrome.Semantic proximity Read ↗

DFNA2/KCNQ4 and its manifestations.Semantic proximity Read ↗

Clinical phenotype of DFN2, DFN4 and DFN6.Semantic proximity Read ↗

Mapping of the DFNB1 locus.Semantic proximity Read ↗

Elevated Risk for MPNST in NF1 Microdeletion PatientsSemantic proximity Read ↗

Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype.Semantic proximity Read ↗

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