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Alagille syndrome: clinical perspectives
Alagille syndrome is an autosomal dominant, complex multisystem disorder characterized by the presence of three out of five major clinical criteria: cholestasis with bile duct paucity on liver biopsy, congenital cardiac defects (with particular involvement of the pulmonary arteries), posterior embry...
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| Vydáno v: | Appl Clin Genet |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Dove Medical Press
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4935120/ https://ncbi.nlm.nih.gov/pubmed/27418850 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S86420 |
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