Autosomal dominant midfrequency hearing impairment

Scandinavian Audiology, Supplement

Volumn 30, Issue 52, 2001, Pages 85-87

  Kaksonen, R ^a,b   Widen, E ^b   Cormand, B ^b   Toppila, E ^c   Starck, J ^c   Pyykko I ^a   Kere, J ^b  

^a KAROLINSKA INSTITUTE   (Sweden)

^b UNIVERSITY OF HELSINKI   (Finland)

^c FINNISH INSTITUTE OF OCCUPATIONAL HEALTH   (Finland)

Author keywords

Autosomal; Dominant; Genetic; Hearing impairment; Midfrequency; Non syndromic

Indexed keywords

ARTICLE; AUDIOGRAPHY; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 11; CHROMOSOME 19; CHROMOSOME 6; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENE LOCUS; HEARING IMPAIRMENT; HUMAN; MALE; ONSET AGE; PEDIGREE; PRIORITY JOURNAL; CHROMOSOME ABERRATION; CHROMOSOME DISORDER; GENETIC POLYMORPHISM; GENETICS; HOSPITALIZATION; PERCEPTION DEAFNESS; PURE TONE AUDIOMETRY;

AUDIOMETRY, PURE-TONE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; PEDIGREE; POLYMORPHISM, GENETIC; SEVERITY OF ILLNESS INDEX;

EID: 0034744864     PISSN: 01078593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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