A syndrome of progessive sensorineual deafness and cataract inherited as an autosomal dominant trait
- Author
- GUALA, A1 ; GERMINETTI, V; SEBASTIANI, F; SILENGO, M. C
[1] Univ. Torino, ist. discipline pediatriche, 10126 Torino, Italy - Source
Clinical genetics. 1992, Vol 41, Num 6, pp 293-295 ; ref : 5 ref
- Publisher
- Blackwell, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Caractère autosomique Caractère dominant Cataracte Etude familiale Homme Maladie héréditaire ORL pathologie Oeil pathologie Oreille interne pathologie Surdité cochléaire Surdité perception Syndrome complexe Cristallin pathologie
- Keyword (en)
- Autosomal character Dominant character Cataract Family study Human Genetic disease ENT disease Eye disease Internal ear disease Sensorineural hearing loss Perception hearing loss Complex syndrome
- Keyword (es)
- Carácter autosómico Carácter dominante Catarata Estudio familiar Hombre Enfermedad hereditaria ORL patología Ojo patología Oido interno patología Sordera coclear Sordera percepción Síndrome complejo
- 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
- 5384244
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
10.1111/j.1399-0004.1992.tb03400.x 
https://dx.doi.org/10.1111/j.1399-0004.1992.tb03400.x
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