Application of the audioscan in the detection of carriers of genetic hearing loss: Original paper

International Journal of Audiology

Volumn 34, Issue 2, 1995, Pages 91-97

  Stephens, Dafydd ^a   Meredith, Rhys ^a   Sirimanna, Tony ^a   France, Liz ^a   Almqvist, Charlotte ^b   Haugen, Hedda ^b  

^a UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

^b LUND UNIVERSITY   (Sweden)

Author keywords

Audioscan; Detection of carriers; Genetic deafness; Non syndromal hearing loss

Indexed keywords

ADULT; ARTICLE; AUDIOMETRY; CONTROLLED STUDY; FATHER; FEMALE; HEARING LOSS; HETEROZYGOTE DETECTION; HUMAN; MAJOR CLINICAL STUDY; MALE; MOTHER; PRIORITY JOURNAL; RECESSIVE INHERITANCE;

ADULT; AUDIOMETRY; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; COMPARATIVE STUDY; FEMALE; HEARING LOSS, SENSORINEURAL; HUMAN; MALE; MIDDLE AGE; PILOT PROJECTS; SEX FACTORS;

EID: 0029121642     PISSN: 14992027     EISSN: None     Source Type: Journal    
DOI: 10.3109/00206099509071902     Document Type: Article

References (12)

1. Deafness as a eugenic problem
2. Audiometric examination of parents of children deaf from birth
3. Audiometric identification of normal hearing carriers of genes for deafness
4. A study of the causes of hearing loss with special reference to genetic factors
5. Audiomérie auto-matique de dépistage préventif: Le balayage fréquentiel asservi (Au-dioscan)
6. Audiometric detection of carriers of Usher's syndrome type II
7. Alport's syndrome: Can the carrier be identified by audiometry
8. The All-Wales Audiology and Genetic Service for Hearing Impaired Young Adults