Prenatal diagnosis of Batten's disease
- Author
- MUNROE, P. B1 ; RAPOLA, J; MITCHISON, H. M1 ; MUSTONEN, A1 ; MOLE, S. E1 ; GARDINER, R. M; JÄRVELÄ, I
[1] Department of Paediatrics, Rayne Institute, University College London Medical School, London, United Kingdom - Source
Lancet (British edition). 1996, Vol 347, Num 9007, pp 1014-1015 ; ref : 9 ref
- CODEN
- LANCAO
- ISSN
- 0140-6736
- Scientific domain
- General medicine general surgery
- Publisher
- Lancet, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Céroïde lipofuscinose neuronale infantile Diagnostic Déterminisme génétique Homme Microscopie électronique Prénatal Anatomopathologie Encéphale pathologie Maladie héréditaire Système nerveux pathologie
- Keyword (en)
- Infantile neuronal ceroid lipofuscinosis Diagnosis Genetic inheritance Human Electron microscopy Prenatal Pathology Cerebral disorder Genetic disease Nervous system diseases
- Keyword (es)
- Ceroide lipofuscinoso neuronal infantil Diagnóstico Determinismo genético Hombre Microscopía electrónica Prenatal Anatomía patológica Encéfalo patología Enfermedad hereditaria Sistema nervioso patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 3051084
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
10.1016/S0140-6736(96)90148-8 
https://dx.doi.org/10.1016/S0140-6736(96)90148-8
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