Journal article
Diagnosis and Molecular Biology of Hereditary Hearing Loss
Otolaryngology-head and neck surgery, Vol.112(5), pp.P102-P102
05/1995
DOI: 10.1016/S0194-5998(05)80249-9
Abstract
Educational objectives: To understand the types of hereditary hearing impairment (autosomal dominant, autosomal recessive, X-linked, mitochondrial, syndromic, nonsyndromic) and the importance of clinical diagnosis in molecular genetic studies of hereditary hearing impairment.
Details
- Title: Subtitle
- Diagnosis and Molecular Biology of Hereditary Hearing Loss
- Creators
- Richard J.H Smith - Iowa City, IowaKenneth M Grundfast - Washington, D.C.
- Resource Type
- Journal article
- Publication Details
- Otolaryngology-head and neck surgery, Vol.112(5), pp.P102-P102
- Publisher
- SAGE Publications
- DOI
- 10.1016/S0194-5998(05)80249-9
- ISSN
- 0194-5998
- eISSN
- 1097-6817
- Language
- English
- Date published
- 05/1995
- Academic Unit
- Internal Medicine; Stead Family Department of Pediatrics; Otolaryngology; Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Iowa Neuroscience Institute
- Record Identifier
- 9984256931202771
Metrics
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