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- Acute treatment of hyperammonemia by continuous renal replacement therapy in a newborn patient with ornithine transcarbamylase deficiency
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- Survival analysis of spinal muscular atrophy type I
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- Clinical Approaches to Genetic Disorders
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- Role of Polymorphism in HLA DQ-α and -β Chain Loci in the Pathophysiology of Autoimmune Thyroid Disease in Children with and without Turner Syndrome
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- Clinical Differences by Karyotype in Patients with Turner Syndrome
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- A Case of Transfusion-Associated Gragt-Verus-Host Disease in a Preterm Infant
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