Clinical evidence of intrauterine disturbance in Prader-Willi syndrome, a genetically imprinted neurodevelopmental disorder
- Author
- DUDLEY, Oenone1 ; MUSCATELLI, F1
[1] NMDA, UMR CNRS 6156, Intitut de Biologie Moléculaire de Luminy (IBDML), Campus de Luminy, Case 907, 13288 Marseille, France - Source
Early human development. 2007, Vol 83, Num 7, pp 471-478, 8 p ; ref : 52 ref
- CODEN
- EHDEDN
- ISSN
- 0378-3782
- Scientific domain
- Embryology, development; Pediatrics; Psychology, psychopathology, psychiatry
- Publisher
- Elsevier, Amsterdam
/
Elsevier, Lausanne
/
Elsevier, New York,NY
- Publication country
- Netherlands
- Document type
- Article
- Language
- English
- Author keyword
- Imprinting Intrauterine Phenotype Prader-Willi syndrome
- Keyword (fr)
- Homme Prader Labhart Willi syndrome Endocrinopathie Maladie héréditaire Syndrome complexe Système ostéoarticulaire pathologie
- Keyword (en)
- Human Prader Labhart Willi syndrome Endocrinopathy Genetic disease Complex syndrome Diseases of the osteoarticular system
- Keyword (es)
- Hombre Prader Labhart Willi síndrome Endocrinopatía Enfermedad hereditaria Síndrome complejo Sistema osteoarticular patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A30 Embryology: invertebrates and vertebrates. Teratology
- Discipline
- Embryology : invertebrates and vertebrates. Teratology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18833875
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
10.1016/j.earlhumdev.2006.09.002 
https://dx.doi.org/10.1016/j.earlhumdev.2006.09.002
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