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Oral phenotype and scoring of vascular Ehlers–Danlos syndrome: a case–control study
OBJECTIVE: Vascular Ehlers–Danlos syndrome (vEDS) is a rare genetic condition related to mutations in the COL3A1 gene, responsible of vascular, digestive and uterine accidents. Difficulty of clinical diagnosis has led to the design of diagnostic criteria, summarised in the Villefranche classificatio...
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| Autors principals: | , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Group
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3323826/ https://ncbi.nlm.nih.gov/pubmed/22492385 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjopen-2011-000705 |
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