Idiopathic arterial calcification of infancy: genetic studies

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Idiopathic arterial calcification of infancy: genetic studies

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Biallelic TXNIP deficiency is associated with a multisystemic metabolic disease.

Correction: Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease.

Extrahepatic biliary atresia and normal-range serum gamma-glutamyltranspeptidase activity: A case report.

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Development of Perinatal Social Determinants of Health Composite Risk Score in Infants Born Preterm.

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Idiopathic arterial calcification of infancy: genetic studies

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