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Endocrine dysfunctions in children with Williams-Beuren syndrome
PURPOSE: Williams-Beuren syndrome (WBS) is caused by a hemizygous microdeletion of chromosome 7q11.23 and is characterized by global cognitive impairment, dysmorphic facial features, and supravalvular aortic stenosis. Endocrine dysfunctions have been reported in patients with WBS. This study was per...
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| Publicado no: | Ann Pediatr Endocrinol Metab |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Korean Society of Pediatric Endocrinology
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4835556/ https://ncbi.nlm.nih.gov/pubmed/27104174 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6065/apem.2016.21.1.15 |
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