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French database of children and adolescents with Prader-Willi syndrome
BACKGROUND: Prader-Willi syndrome (PWS) is a rare multisystem genetic disease leading to severe complications mainly related to obesity. We strongly lack information on the natural history of this complex disease and on what factors are involved in its evolution and its outcome. One of the objective...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2569911/ https://ncbi.nlm.nih.gov/pubmed/18831731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-9-89 |
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