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Article

[Hereditary deafness in Turkey. Initial results].

HNO - 1 Sept 1998

Apaydin F, Pfister M, Iber M, Kandogan T, Leal S M, Brändle U, Cura O, Zenner H P

Abstract excerpt

The authors describe a study in progress to identify Turkish families with hereditary hearing loss and isolate possible responsible disease genes. Due to extreme genetic heterogeneity and limited audiological differentiation of hereditary hearing loss, it is necessary to identify large or small f...

Topics

Child
Chromosome Aberrations
Chromosome Disorders
Consanguinity
Deafness
Female
Genes, Dominant
Genes, Recessive
Genetic Predisposition to Disease
Genetic Testing
Humans
Male
Pedigree

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Risk Factors

Sex Chromosome Aberrations

Syndrome

Turkey

X Chromosome

Source

Open in PubMed Open full text

Identifiers

PMID: 9816535
DOI: 10.1007/s001060050317
PMCID: PMC6181136

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9816535-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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