Résultat(s) 1 - 5 résultats de 5 pour la requête 'Huang, Yonglan', Temps de recherche: 2,75s Affiner les résultats
  1. 1
    Clinical and molecular analysis of two Chinese siblings with Cockayne syndrome
    Autres auteurs: “...Huang, Yonglan...”

    Article en ligne

  2. 2
    Application of dried blood spot method in screening Gaucher's disease
    Autres auteurs: “...Huang, Yonglan...”
    Article

  3. 3
    Analysis of clinical features and arylsulfatase B gene mutation in thirteen Chinese children with mucopolysaccharidosis type VI
    Autres auteurs: “...Huang, Yonglan...”
    Article

  4. 4
    A novel homozygous mutation p.E25X in the HSD3B2 gene causing salt wasting 3β-hydroxysteroid dehydrogenases deficiency in a Chinese pubertal girl a delayed diagnosis until recurrent ovary cysts
    Article

  5. 5
    Clinical and molecular characteristics of a child with juvenile Sandhoff disease
    Article

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