This article describes the hearing impairment (HI) phenotype which segregates in a large multi-generation Swiss-German family with autosomal dominant nonsyndromic HI. The locus segregating within this pedigree is located on chromosome 4q35-qter and is designated as DFNA24. For this pedigree, audiometric data on 25 hearing-impaired family members are available. It was demonstrated that within this kindred the HI is sensorineural, bilateral, prelingual in onset, and progressive throughout life. Age-related typical audiograms depict steeply down-sloping curves, with moderate high-frequency HI at birth, then steady progression to moderate HI in the low frequencies, severe HI at mid-frequencies and profound HI at high frequencies by age 70. Annu...
OBJECTIVES: To perform linkage analysis and to outline hearing loss characteristics in a family exhi...
Item does not contain fulltextWe present a detailed analysis of the DFNA10 phenotype based on data f...
We present a detailed analysis of the DFNA10 phenotype based on data from 25 hearing-impaired person...
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...
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-gener...
Item does not contain fulltextThis article describes the hearing impairment (HI) phenotype which seg...
Nonsyndromic hearing loss is one of the most genetically heterogeneous traits known. A total of 30 a...
Nonsyndromic hearing loss is one of the most genetically heterogeneous traits known. A total of 30 a...
Nonsyndromic hearing loss is one of the most genetically heterogeneous traits known. A total of 30 a...
DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss Ge...
Using linkage analysis, we identified a novel dominant locus, DFNA25, for delayed-onset, progressive...
DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss Ge...
DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss Ge...
OBJECTIVE: To delineate the phenotype and genotype of an autosomal dominant low-frequency sensorineu...
OBJECTIVES: To perform linkage analysis and to outline hearing loss characteristics in a family exhi...
Item does not contain fulltextWe present a detailed analysis of the DFNA10 phenotype based on data f...
We present a detailed analysis of the DFNA10 phenotype based on data from 25 hearing-impaired person...
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...
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-gener...
Item does not contain fulltextThis article describes the hearing impairment (HI) phenotype which seg...
Nonsyndromic hearing loss is one of the most genetically heterogeneous traits known. A total of 30 a...
Nonsyndromic hearing loss is one of the most genetically heterogeneous traits known. A total of 30 a...
Nonsyndromic hearing loss is one of the most genetically heterogeneous traits known. A total of 30 a...
DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss Ge...
Using linkage analysis, we identified a novel dominant locus, DFNA25, for delayed-onset, progressive...
DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss Ge...
DFNA23, a novel locus for autosomal dominant nonsyndromic hearing loss, was identified in a Swiss Ge...
OBJECTIVE: To delineate the phenotype and genotype of an autosomal dominant low-frequency sensorineu...
OBJECTIVES: To perform linkage analysis and to outline hearing loss characteristics in a family exhi...
Item does not contain fulltextWe present a detailed analysis of the DFNA10 phenotype based on data f...
We present a detailed analysis of the DFNA10 phenotype based on data from 25 hearing-impaired person...