Incidence and prevalence of the 22q11 deletion syndrome: A population-based study in Western sweden
- Author
- OSKARSDOTTIR, S1 ; VUJIC, M2 ; FASTH, A1
[1] Department of Paediatrics, Göteborg University, Gothenburg, Sweden
[2] Department of Clinical Genetics, Göteborg University, Gothenburg, Sweden - Source
Archives of disease in childhood. 2004, Vol 89, Num 2, pp 148-151, 4 p ; ref : 15 ref
- CODEN
- ADCHAK
- ISSN
- 0003-9888
- Scientific domain
- Pediatrics
- Publisher
- BMJ, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Chromosome G22 Délétion Enfant Epidémiologie Incidence Prévalence Pédiatrie Suède Homme Europe
- Keyword (en)
- Chromosome G22 Deletion Child Epidemiology Incidence Prevalence Pediatrics Sweden Human Europe
- Keyword (es)
- Cromosoma G22 Deleción Niño Epidemiología Incidencia Prevalencia Pediatría Suecia Hombre Europa
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23B Chromosome aberrations
- Discipline
- Generalities in medical sciences Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 15456623
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.2003.026880 
https://dx.doi.org/10.1136/adc.2003.026880
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