Presenting phenotype in 100 children with the 22q11 deletion syndrome
- Author
- OSKARSDOTTIR, Solveig1 ; PERSSON, Christina2 ; ERIKSSON, Bengt O1 ; FASTH, Anders1
[1] Department of Paediatrics, The Queen Silvia Children's Hospital, 416 85 Göteborg, Sweden
[2] Department of Logopaedics and Phoniatrics, Sahlgrenska Academy, Göteborg University, Göteborg, Sweden - Source
European journal of pediatrics. 2005, Vol 164, Num 3, pp 146-153, 8 p ; ref : 18 ref
- CODEN
- EJPEDT
- ISSN
- 0340-6199
- Scientific domain
- Genetics; Pediatrics
- Publisher
- Springer, Berlin
/
Springer, Heidelberg
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Author keyword
- 22q11 deletion DiGeorge syndrome Phenotype Practice guidelines Velocardiofacial syndrome
- Keyword (fr)
- Chromosome G22 Délétion Enfant Immunodéficit héréditaire DiGeorge Phénotype Pratique professionnelle Pédiatrie Recommandation Syndrome Vélocardiofacial syndrome Homme Immunopathologie
- Keyword (en)
- Chromosome G22 Deletion Child DiGeorge syndrome Phenotype Professional practice Pediatrics Recommendation Syndrome Velocardiofacial syndrome Human Immunopathology
- Keyword (es)
- Cromosoma G22 Deleción Niño Inmunodeficiencia hereditaria DiGeorge Fenotipo Práctica profesional Pediatría Recomendación Síndrome Velocardiofacial síndrome Hombre Inmunopatología
- 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
- 16534709
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
10.1007/s00431-004-1577-8 
https://dx.doi.org/10.1007/s00431-004-1577-8
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