Wiedemann-Beckwith syndrome in one of monozygotic twins
- Author
- BOSE, B1 ; WILKIE, R. A; MADLOM, M; FORSYTH, J. S; FAED, M. J. W
[1] Ninewells hosp. medical school, Dundee DD1 9SY, United Kingdom - Source
Archives of disease in childhood. 1985, Vol 60, Num 12, pp 1191-1192 ; ref : 6 ref
- CODEN
- ADCHAK
- ISSN
- 0003-9888
- Scientific domain
- Pediatrics
- Publisher
- BMJ, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Beckwith Wiedemann syndrome Concordance discordance Enfant Hypoglycémie Jumeau monozygote Macroglossie Omphalocèle Syndrome complexe Homme
- Keyword (en)
- Beckwith Wiedemann syndrome Concordance discordance Child Hypoglycemia Monozygotic twin Macroglossia Omphalocele Complex syndrome Human
- Keyword (es)
- Beckwith Wiedemann sindrome Concordancia discordancia Niño Hipoglucemia Gemelo monozigotico Macroglosia Onfalocele Síndrome complejo Hombre
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23E Complex syndromes
- Discipline
- Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 7938451
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.60.12.1191 
https://dx.doi.org/10.1136/adc.60.12.1191
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