Prader-Willi Syndrome: Clinical Aspects

Prader-Willi Syndrome (PWS) is a complex multisystem genetic disorder that shows great variability, with changing clinical features during a patient's life. The syndrome is due to the loss of expression of several genes encoded on the proximal long arm of chromosome 15 (15q11.2–q13). The comple...

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Detalles Bibliográficos
Autores principales: Elena, Grechi, Bruna, Cammarata, Benedetta, Mariani, Stefania, Di Candia, Giuseppe, Chiumello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3486015/
https://www.ncbi.nlm.nih.gov/pubmed/23133744
http://dx.doi.org/10.1155/2012/473941

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3486015/
https://www.ncbi.nlm.nih.gov/pubmed/23133744
http://dx.doi.org/10.1155/2012/473941

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