We present a detailed analysis of the DFNA10 phenotype based on data from 25 hearing-impaired persons coming from a large American pedigree segregating for deafness at the DFNA10 locus (chromosome 6q22.3-23.2). Cross-sectional analysis of air conduction threshold-on-age data from all available last-visit audiograms (linear regression analysis, age over 15 years) showed progression of hearing loss at a rate of 0.6 dB/y over all frequencies, with a flat to gently sloping age-corrected threshold of about 50 dB. The results were significant at 0.25, 4, and 8 kHz, but only if corrections for presbycusis were not included. Longitudinal threshold analysis performed in 1 case, covering ages 6 to 32 years, showed progression of hearing loss at a rat...
Item does not contain fulltextSpeech recognition scores were analyzed in 34 carriers of a DFNA5 muta...
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-gener...
OBJECTIVE: To assess the audiometric profile and speech recognition characteristics in affected memb...
Item does not contain fulltextWe present a detailed analysis of the DFNA10 phenotype based on data f...
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-gener...
OBJECTIVE: To analyze the phenotype in a 5-generation DFNA13 family with a missense mutation in the ...
OBJECTIVES: To perform linkage analysis and to outline hearing loss characteristics in a family exhi...
Item does not contain fulltextThis article describes the hearing impairment (HI) phenotype which seg...
A total of 64 loci for autosomal dominant non-syndromic hearing impairment have been described, and ...
Speech recognition scores were analyzed in 34 carriers of a DFNA5 mutation. Cross-sectional linear r...
Speech recognition scores were analyzed in 34 carriers of a DFNA5 mutation. Cross-sectional linear r...
Speech recognition scores were analyzed in 34 carriers of a DFNA5 mutation. Cross-sectional linear r...
OBJECTIVE: To delineate the phenotype and genotype of an autosomal dominant low-frequency sensorineu...
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-gener...
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-gener...
Item does not contain fulltextSpeech recognition scores were analyzed in 34 carriers of a DFNA5 muta...
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-gener...
OBJECTIVE: To assess the audiometric profile and speech recognition characteristics in affected memb...
Item does not contain fulltextWe present a detailed analysis of the DFNA10 phenotype based on data f...
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-gener...
OBJECTIVE: To analyze the phenotype in a 5-generation DFNA13 family with a missense mutation in the ...
OBJECTIVES: To perform linkage analysis and to outline hearing loss characteristics in a family exhi...
Item does not contain fulltextThis article describes the hearing impairment (HI) phenotype which seg...
A total of 64 loci for autosomal dominant non-syndromic hearing impairment have been described, and ...
Speech recognition scores were analyzed in 34 carriers of a DFNA5 mutation. Cross-sectional linear r...
Speech recognition scores were analyzed in 34 carriers of a DFNA5 mutation. Cross-sectional linear r...
Speech recognition scores were analyzed in 34 carriers of a DFNA5 mutation. Cross-sectional linear r...
OBJECTIVE: To delineate the phenotype and genotype of an autosomal dominant low-frequency sensorineu...
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-gener...
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-gener...
Item does not contain fulltextSpeech recognition scores were analyzed in 34 carriers of a DFNA5 muta...
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-gener...
OBJECTIVE: To assess the audiometric profile and speech recognition characteristics in affected memb...