Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qter
- Author
- GREGG, R. G; METZENBERG, A. B; HOGAN, K; SEKHON, G; LAXOVA, R
Univ. Wisconsin-Madison, Waisman cent. mental retardation human development, Madison WI 53706, United States - Source
Genomics (San Diego, Calif.). 1991, Vol 9, Num 4, pp 701-706, 6 p ; ref : 25 ref
- ISSN
- 0888-7543
- Scientific domain
- Cell biology, histology; Genetics
- Publisher
- Elsevier, San Diego, CA
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Arriération mentale Carte génétique Chromosome X Homme Linkage Maladie héréditaire Marqueur génétique Parkinson maladie Polymorphisme longueur fragment restriction Système nerveux pathologie Waisman syndrome
- Keyword (en)
- Mental retardation Genetic mapping X-Chromosome Human Linkage Genetic disease Genetic marker Parkinson disease Restriction fragment length polymorphism Nervous system diseases
- Keyword (es)
- Retraso mental Mapa genético Cromosoma X Hombre Ligamiento Enfermedad hereditaria Marcador genético Parkinson enfermedad Polimorfismo longitud fragmento restricción 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
- 19656552
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
10.1016/0888-7543(91)90363-J 
https://dx.doi.org/10.1016/0888-7543(91)90363-J
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