What is included with this book?
Dafydd Stephens FRCP, is Honorary Professor of Audiological Medicine at Cardiff University, Wales, UK. Sophia E. Kramer, PhD, is Senior Researcher and Psychologist at the Department of E.N.T. / Audiology / EMGO Institute for Health and Care Research at the VU University Medical Centre in Amsterdam, the Netherlands.
Preface | |
Contributors | |
Gene therapy | |
Gene therapy for hearing disorders | |
Radiology | |
Radiology of inner ear defects | |
Computer Systems | |
An Internet database on genetic non-syndromal hearing impairments | |
A decision support system for the diagnosis of syndromal genetic hearing impairment | |
Epidemiology | |
Epidemiology of hereditary hearing impairment in childhood - preliminary estimates from the European Union | |
The German Registry for Hearing Impairment in Children: preliminary results | |
Recessive hearing impairment in two birth cohorts in western Sicily | |
Aetiology of hearing impairment in children borth in northern Finland ijn 1975-1979 and in 1985-1989 (Abstract) | |
Audiovestibular tests | |
Audiometric criteria for linkage analysis in genetic hearing impairment | |
Audioscan notches in carriers of genetic hearing impairment | |
Cochlear irregulatities in obligate carriers of recessive genetic hearing impairment and in control subjects | |
Three-dimensional video-oculography for the detection of genetic vestibular dysfunction at the level of the threee semicircular canals and the otoliths (Abstract) | |
Non-syndromal autosomal recessive hearing impairment | |
Homozygosity mapping applied to hereditary hearing impairment - localizing recessive deafness genes | |
A Turkish kindred with autosomal recessive non-syndromal hearing impairment segregates DFNB9 (Abstract) | |
Assessment of the contribution of the loci DFNA1-10 and DFNB1-9 in inherited hearing impairment in two populations: The United Arab Emirates and the British Pakistani populations (Abstract) | |
Non-syndromal autosomal dominant hearing impairment | |
Hereditary dominant non-syndromal progressive hearing impairment in a large family in southern Italy | |
Autosomal dominant non-syndromal progressive sensorineural hearing impairment: audiological evalution of a Dutch DFNA2 family (Abstract) | |
Autosomal dominant congenital severe sensorineural hearing impairment - localization of a disease gene to chromosome 11q by linkage in an Austrian family (Abstract) | |
X-Linked hearing impairment Chapter | |
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