Résultat(s) 1 - 12 résultats de 12 pour la requête 'Qiu, Zheng-qing', Temps de recherche: 1,47s Affiner les résultats
  1. 1
    Gene analysis and literature review of autosomal recessive polycystic kidney disease
    Autres auteurs: “...Qiu, Zheng-qing...”
    Article

  2. 2
    Clinical characterization and mutation identification for multiple sulfatase deficiency patients in China
    Autres auteurs: “...Qiu, Zheng-qing...”
    Article

  3. 3
    The importance of confirmative diagnosis of presymptomatic patients with Wilson's disease
    Article

  4. 4
    Clinical sequelae of 17 cases with glycogen storage disease type II/Pompe disease
    Autres auteurs: “...Qiu, Zheng-qing...”
    Article

  5. 5
    Mutation analysis and prenatal diagnosis of 2 cases with mucopolysaccharidosis type I
    Autres auteurs: “...Qiu, Zheng-Qing...”
    Article

  6. 6
    Mutation in the SLC37A4 gene of glycogen storage disease type Ib in 15 families of the mainland of China
    Article

  7. 7
    Diagnosis of glycogen storage disease type IIIA by detecting glycogen debranching enzyme activity, glycogen content and structure in muscle
    Autres auteurs: “...Qiu, Zheng-qing...”
    Article

  8. 8
    Postnatal and prenatal diagnosis of mucopolysaccharidosis type III (Sanfilippo syndrome)
    Autres auteurs: “...Qiu, Zheng-qing...”
    Article

  9. 9
    A brief introduction to the 10th Annual Asian Symposium on lysosomal storage disease
    Article

  10. 10
    Mutation analysis of glycogen debrancher enzyme gene in five Chinese patients with glycogen storage disease type III
    Autres auteurs: “...Qiu, Zheng-qing...”
    Article

  11. 11
    A Chinese girl with cleidocranial dysplasia (CCD) caused by the recurrent R190W mutation in RUNX 2
    Article

  12. 12
    Heterogeneous phenotypes in Chinese glycogen storage disease type Ia patients with homozygous G727T mutation
    Article

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