Usher syndrome: clinical findings and gene localization studies
- Author
- KIMBERLING, W. J1 ; MÖLLER, C. G; DAVENPORT, S. L. H; LUND, G; GRISSOM, T. J; PRILUCK, I; WHITE, V; WESTON, M. D; BISCONE-HALTERMAN, K; BROOKHOUSER, P. E
[1] Boys Town national inst. communication disorders children, Omaha NE 68131, United States - Source
The Laryngoscope. 1989, Vol 99, Num 1, pp 66-72 ; ref : 31 ref
- CODEN
- LARYA8
- ISSN
- 0023-852X
- Scientific domain
- Otorhinolaryngology, stomatology, dentistry
- Publisher
- Wiley-Blackwell, Honboken, NJ
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Gène Homme Héréditaire Localisation ORL pathologie Oeil pathologie Rétinite pigmentaire Surdité Usher syndrome
- Keyword (en)
- Gene Human Hereditary Localization ENT disease Eye disease Retinitis pigmentosa Hearing loss Usher syndrome
- Keyword (es)
- Gen Hombre Hereditario Localización ORL patología Ojo patología Retinitis pigmentaria Sordera Usher síndrome
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23E Complex syndromes
- Discipline
- Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 7101723
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1288/00005537-198901000-00013 
https://dx.doi.org/10.1288/00005537-198901000-00013
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