Literature DB >> 983683

Identification of normal hearing carriers of genes for deafness.

H Anderson, E Wedenberg.   

Abstract

The dominant and sex-linked forms of hereditary hearing loss, which have long been recognized, are readily identified on the basis of the family history and routine hearing tests. The mode of inheritance of the recessive forms of hereditary deafness, on the other hand, has been extremely difficult to determine. The research of the last few years, however, has disclosed that carriers of genes for recessive deafness can be identified by audiometric recording of certain peculiarities in the hearing function. This is an important advance, not only as regards diagnositc work, but also in the research into the genetics of deafness.

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Year:  1976        PMID: 983683     DOI: 10.3109/00016487609120895

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN: 0001-6489            Impact factor:   1.494


  3 in total

Review 1.  Genetic deafness.

Authors:  W Reardon
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

2.  [Hereditary deafness in Turkey. Initial results].

Authors:  F Apaydin; M Pfister; M Iber; T Kandogan; S M Leal; U Brändle; O Cura; H P Zenner
Journal:  HNO       Date:  1998-09       Impact factor: 1.284

3.  Audiometric evaluation of carriers of the connexin 26 mutation 35delG.

Authors:  Annamaria Franzé; Antonella Caravelli; Francesca Di Leva; Elio Marciano; Gennaro Auletta; Federica D'Aulos; Claudio Saulino; Laura Esposito; Massimo Carella; Paolo Gasparini
Journal:  Eur Arch Otorhinolaryngol       Date:  2005-05-14       Impact factor: 2.503

  3 in total

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