A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss

American Journal of Otology

Volumn 19, Issue 6, 1998, Pages 718-723

  Govaerts, Paul J ^a   De Ceulaer, Geert ^a   Daemers, Kristin ^a   Verhoeven, Kristien ^b   Van Camp, Guy ^b   Schatteman, Isabelle ^b   Verstreken, Margriet ^b   Willems, Patrick J ^b   Somers, Thomas ^a   Offeciers, F Erwin ^a  

^a SINT AUGUSTINUS HOSPITAL   (Belgium)

^b UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

Audiology; Autosomal dominant; Genetics; Midfrequency; Sensorineural hearing loss

Indexed keywords

ARTICLE; AUDIOLOGY; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 11Q; CHROMOSOME MAP; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; GENE EXPRESSION; GENE LOCUS; GENETIC LINKAGE; HEARING LOSS; HUMAN; PATIENT REFERRAL; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PURE TONE AUDIOMETRY; STANDARDIZATION; STATISTICAL ANALYSIS;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; ANALYSIS OF VARIANCE; AUDIOMETRY, PURE-TONE; BIAS (EPIDEMIOLOGY); CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; DISCRIMINANT ANALYSIS; FEMALE; GENES, DOMINANT; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MIDDLE AGED; PEDIGREE; REPRODUCIBILITY OF RESULTS; RETROSPECTIVE STUDIES; SENSITIVITY AND SPECIFICITY;

EID: 0031793315     PISSN: 01929763     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. Verhoeven K, Van Camp G, Govaerts PJ, et al. A gene for autosomal dominant non-syndromic hearing loss (DFNA12) maps to chromosome 11q22-24. Am J Hum Genet 1997;60:1168-73.
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7. Govaerts PJ, Somers Th, Offeciers FE. Box and Whisker plots for graphic presentation of audiometric results of conductive hearing loss treatment. Otolaryngol Head Neck Surg 1998;118: 892-5.