Genetic Epidemiology of Deafness
- 10 April 2006
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 53 references indexed in Scilit:
- Fine Mapping of the Human Biotinidase Gene and Haplotype Analysis of Five Common MutationsHuman Heredity, 1999
- Evidence for Digenic Inheritance of Nonsyndromic Hereditary Hearing Loss in a Swedish FamilyAmerican Journal of Human Genetics, 1998
- Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsHuman Genetics, 1998
- Mutation of the Gene for I sK Associated With Both Jervell and Lange-Nielsen and Romano-Ward Forms of Long-QT SyndromeCirculation, 1998
- Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian familyHuman Molecular Genetics, 1996
- Mitochondrial mutation associated with nonsyndromic deafnessAmerican Journal of Otolaryngology, 1995
- Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4Science, 1995
- Autosomal recessive non-syndromal progressive sensorineural deafness in childhood. A separate clinical and genetic entityInternational Journal of Pediatric Otorhinolaryngology, 1979
- A Model for Transducer Action in the CochleaPublished by Cold Spring Harbor Laboratory ,1965
- A NOTE ON DEAF MUTISMAnnals of Human Genetics, 1959