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Testing carrier status in siblings of patients with cystic fibrosis

Author
BALFOUR-LYNN, I; MADGE, S; DINWIDDIE, R
NHS Trust, hosp. children, respiratory unit, London WC1N 3JH, United Kingdom
Source

Archives of disease in childhood. 1995, Vol 72, Num 2, pp 167-168 ; ref : 5 ref

CODEN
ADCHAK
ISSN
0003-9888
Scientific domain
Pediatrics
Publisher
BMJ, London
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Dépistage Enfant Ethique Génotype Hétérozygotie Mucoviscidose Appareil digestif pathologie Appareil respiratoire pathologie Homme Maladie héréditaire Métabolisme pathologie Pancréas pathologie
Keyword (en)
Medical screening Child Ethics Genotype Heterozygozity Cystic fibrosis Digestive diseases Respiratory disease Human Genetic disease Metabolic diseases Pancreatic disease
Keyword (es)
Descubrimiento Niño Etica Genotipo Heterozigosis Mucoviscidosis Aparato digestivo patología Aparato respiratorio patología Hombre Enfermedad hereditaria Metabolismo patología Páncreas patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D05 Miscellaneous hereditary metabolic disorders

Discipline
Metabolic diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
3418574

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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