Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosis
- Author
- LEMNA, W. K; FELDMAN, G. L; KEREM, B; FERNBACH, S. D; ZEVKOVICH, E. P; O'BRIEN, W. E; RIORDAN, J. R; COLLINS, F. S; LAP-CHEE TSUI; BEAUDET, A. L
Baylor coll. medicine, Howard Hughes medical inst., Houston TX 77030, United States - Source
The New England journal of medicine. 1990, Vol 322, Num 5, pp 291-296 ; ref : 24 ref
- CODEN
- NEJMAG
- ISSN
- 0028-4793
- Scientific domain
- General medicine general surgery
- Publisher
- Massachusetts Medical Society, Boston, MA
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Cytogénétique Exploration Foetus Homme Mucoviscidose Métabolisme pathologie
- Keyword (en)
- Cytogenetics Exploration Fetus Human Mucoviscidosis Metabolic diseases
- Keyword (es)
- Citogenética Exploración Feto Hombre Mucoviscidosis Metabolismo patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B24 Investigative techniques, diagnostic techniques (general aspects) / 002B24O Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
- Discipline
- Scanning and diagnostic techniques
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4619098
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
10.1056/NEJM199002013220503 
https://dx.doi.org/10.1056/NEJM199002013220503
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