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Prader–Willi Syndrome and Hypogonadism: A Review Article
Prader-Labhart-Willi syndrome (PWS) is a rare genetic disorder characterized by intellectual disability, behavioural problems, hypothalamic dysfunction and specific dysmorphisms. Hypothalamic dysfunction causes dysregulation of energy balance and endocrine deficiencies, including hypogonadism. Altho...
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| Foilsithe in: | Int J Mol Sci |
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| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
MDPI
2021
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7962179/ https://ncbi.nlm.nih.gov/pubmed/33800122 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22052705 |
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