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Prader–Willi syndrome
Prader–Willi syndrome (PWS) is a highly variable genetic disorder affecting multiple body systems whose most consistent major manifestations include hypotonia with poor suck and poor weight gain in infancy; mild mental retardation, hypogonadism, growth hormone insufficiency causing short stature for...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2009
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2985966/ https://ncbi.nlm.nih.gov/pubmed/18781185 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2008.165 |
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