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Preimplantation genetic testing for Huntington disease and certain other dominantly inherited disorders

Author
SCHULMAN, J. D1 ; BLACK, S. H1 ; HANDYSIDE, A; NANCE, W. E
[1] Genetics & IVF Institute, 3020 Javier Road, Fairfax, VA 22031, United States
Source

Clinical genetics. 1996, Vol 49, Num 2, pp 57-58 ; ref : 6 ref

CODEN
CLGNAY
ISSN
0009-9163
Scientific domain
Genetics
Publisher
Blackwell, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Blastocyste Chorée Huntington Diagnostic Fécondation in vitro transfert embryon Homme Prénatal Encéphale pathologie Extrapyramidal syndrome Maladie dégénérative Maladie héréditaire Système nerveux central pathologie Système nerveux pathologie
Keyword (en)
Blastocyst Huntington disease Diagnosis In vitro fertilization embryo transfer Human Prenatal Cerebral disorder Extrapyramidal syndrome Degenerative disease Genetic disease Central nervous system disease Nervous system diseases
Keyword (es)
Blastocisto Corea Huntington Diagnóstico Fecundación in vitro transplante embrión Hombre Prenatal Encéfalo patología Extrapiramidal síndrome Enfermedad degenerativa Enfermedad hereditaria Sistema nervosio central patología 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
3049751

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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