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Article

Further evidence for linkage of low-mid frequency hearing impairment to the candidate region on chromosome 4p16.3.

Clinical genetics - 1 Aug 2001

Brodwolf S, Böddeker I R, Ziegler A, Rausch P, Kunz J

Abstract excerpt

We have investigated a three-generation family with an autosomal dominant low-mid frequency hearing loss. Audiograms show consistently a hearing threshold of 50+/-20 db hearing loss (HL) between 250 Hz and 1-2 kHz. Normal hearing level was reached between 3 and 6 kHz in all examined children. Adult patients show an additional hearing impairment (HI) in the mid and higher frequencies that seems to differ from...

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Source

Identifiers

PMID: 11553051
DOI: 10.1034/j.1399-0004.2001.600211.x

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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

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Research trail→

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Further evidence for linkage of low-mid frequency hearing impairment to the candidate region on chromosome 4p16.3.PMID 11553051Read ↗

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[Phenotypic characterization of a DFNA6 family with low-frequency hearing loss].Semantic proximity Read ↗

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

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Two families with phenotypically different hereditary low frequency hearing impairment: longitudinal data and linkage analysis.Semantic proximity Read ↗

A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus.Semantic proximity Read ↗

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