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  1. 1
    Genotype and phenotype analysis of neonates with neonatal encephalopathy complicated with perinatal hypoxic event

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  2. 2
    Infant with 3β-hydroxy-Δ(5)-C27 steroid dehydrogenase deficiency report of two cases and literatures review
    Article

  3. 3
    Clinical features of a Chinese infant with inborn error of bile acid metabolism-3β-hydroxy-Δ(5)-C27-steroid dehydrogenase deficiency and review of the literature
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  4. 4
    Homology modeling and molecular dynamics simulation studies of human type 1 3β-hydroxysteroid dehydrogenase Toward the understanding of cofactor specificity

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  5. 5
    Testicular functions in pubescent and adult patients with cryptorchidism--comparison between descended and undescended sides
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