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pro vyhledávání: '"Odai Jamaan, Alqahtani"'
Publikováno v:
American Journal of Case Reports. 23
BACKGROUND Alagille syndrome (AGS) is a rare genetic disease characterized by 5 typical features: peculiar facial anomaly, posterior embryotoxon, chronic cholestasis, butterfly-like vertebral-arch defects, and cardiovascular malformations. AGS in a l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc5a148842770fe0ae0ac2f82508ed72
https://doi.org/10.12659/ajcr.936513
https://doi.org/10.12659/ajcr.936513
