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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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