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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DOI
10.1136/adc.72.2.167 
https://dx.doi.org/10.1136/adc.72.2.167
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