Résultat(s) 1 - 12 résultats de 12 pour la requête 'Qiu, Zheng-qing', Temps de recherche: 2,11s 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 in the SLC37A4 gene of glycogen storage disease type Ib in 15 families of the mainland of China
    Article

  6. 6
    Mutation analysis and prenatal diagnosis of 2 cases with mucopolysaccharidosis type I
    Autres auteurs: “...Qiu, Zheng-Qing...”
    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
    A brief introduction to the 10th Annual Asian Symposium on lysosomal storage disease
    Article

  9. 9
    Postnatal and prenatal diagnosis of mucopolysaccharidosis type III (Sanfilippo syndrome)
    Autres auteurs: “...Qiu, Zheng-qing...”
    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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