Clinical features and natural history of Beckwith-Wiedemann syndrome : presentation of 74 new cases
- Author
- ELLIOTT, M1 ; BAYLY, R; COLE, T; TEMPLE, I. K; MAHER, E. R1
[1] Addenbrooke's hosp., dep. clin. genetics, Cambridge CB2 2QQ, United Kingdom - Source
Clinical genetics. 1994, Vol 46, Num 2, pp 168-174 ; ref : 25 ref
- Publisher
- Blackwell, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Beckwith Wiedemann syndrome Complication Homme Phénotype Pénétrance génique Appareil urinaire pathologie Endocrinopathie Gigantisme Maladie congénitale Maladie héréditaire Malformation Peau pathologie Stomatologie Syndrome complexe Système ostéoarticulaire pathologie
- Keyword (en)
- Beckwith Wiedemann syndrome Complication Human Phenotype Gene penetrance Urinary system disease Endocrinopathy Gigantism Congenital disease Genetic disease Malformation Skin disease Stomatology Complex syndrome Diseases of the osteoarticular system
- Keyword (es)
- Beckwith Wiedemann síndrome Complicación Hombre Fenotipo Penetrancia génica Aparato urinario patología Endocrinopatía Gigantismo Enfermedad congénita Enfermedad hereditaria Malformación Piel patología Estomatología Síndrome complejo Sistema osteoarticular patología
- 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
- 4216831
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
10.1111/j.1399-0004.1994.tb04219.x 
https://dx.doi.org/10.1111/j.1399-0004.1994.tb04219.x
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