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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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