Neuronally-expressed necdin gene: an imprinted candidate gene in Prader-Willi syndrome
- Author
- SUTCLIFFE, J. S1 ; HAN, M2 ; CHRISTIAN, S. L2 ; LEDBETTER, D. H2
[1] Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN 37232, United States
[2] Center for Medical Genetics, University of Chicago, Chicago, IL, United States - Source
Lancet (British edition). 1997, Vol 350, Num 9090, pp 1520-1521 ; ref : 5 ref
- CODEN
- LANCAO
- ISSN
- 0140-6736
- Scientific domain
- General medicine general surgery
- Publisher
- Lancet, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Déterminisme génétique Homme Prader Labhart Willi syndrome Endocrinopathie Maladie héréditaire Syndrome complexe Système ostéoarticulaire pathologie
- Keyword (en)
- Genetic determinism Human Prader Labhart Willi syndrome Endocrinopathy Genetic disease Complex syndrome Diseases of the osteoarticular system
- Keyword (es)
- Determinismo genético Hombre Prader Labhart Willi síndrome Endocrinopatía Enfermedad hereditaria 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
- 2070344
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/S0140-6736(05)63943-8 
https://dx.doi.org/10.1016/S0140-6736(05)63943-8
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