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70 积分 2026-01-07 加入
Literature review on genotype–phenotype correlation in patients with hereditary spherocytosis
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Erythropoietic Protoporphyria with cirrhosis with late onset dermatological manifestations in an Indian patient- The first report
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Unearthing TULP3 Mutation as a Rare Cause of Cryptogenic Cirrhosis: A Case Report and Review of the Literature
1个月前
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First Indian Case of Wilson's Disease With a Chinese-specific ATP7B Variant: Clinical and Genetic Insights
1个月前
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Bile Duct Paucity in a Case of Neonatal Intrahepatic Cholestasis Due to Citrin Deficiency: Finding the Missing Piece of the Puzzle!
1个月前
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