Möbius' syndrome : Features and etiology
- Author
- GHABRIAL, R1 ; VERSACE, P1 ; KOURT, G1 ; LIPSON, A2 ; MARTIN, F1
[1] Department of Ophthalmology, The New Children's Hospital, Westmead, Australia
[2] Department of Genetics, The New Children's Hospital, Westmead, Australia - Source
Journal of pediatric ophthalmology and strabismus. 1998, Vol 35, Num 6, pp 304-311 ; ref : 18 ref
- CODEN
- JPOSDR
- ISSN
- 0191-3913
- Scientific domain
- Ophthalmology; Pediatrics
- Publisher
- Slack, Thorofare, NJ
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Diplégie faciale congénitale Moebius Enfant Etiologie Exploration clinique Symptomatologie Homme Maladie congénitale Malformation Nerf crânien pathologie Système nerveux central pathologie Système nerveux pathologie
- Keyword (en)
- Moebius syndrome Child Etiology Clinical investigation Symptomatology Human Congenital disease Malformation Cranial nerve disease Central nervous system disease Nervous system diseases
- Keyword (es)
- Diplejía facial congénita Moebius Niño Etiología Exploración clínica Sintomatología Hombre Enfermedad congénita Malformación Nervio craneal patología Sistema nervosio central patología Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17A Nervous system (semeiology, syndromes) / 002B17A08 Cranial nerves. Spinal roots. Peripheral nerves. Autonomic nervous system. Gustation. Olfaction
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 1614584
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
10.3928/0191-3913-19981101-04 
https://dx.doi.org/10.3928/0191-3913-19981101-04
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