Treffer 1 - 12 von 12 für Suche 'Qiu, Zheng-qing', Suchdauer: 5,82s Treffer weiter einschränken
  1. 1
    Gene analysis and literature review of autosomal recessive polycystic kidney disease
    Weitere Verfasser: “...Qiu, Zheng-qing...”
    Aufsatz

  2. 2
    Clinical characterization and mutation identification for multiple sulfatase deficiency patients in China
    Weitere Verfasser: “...Qiu, Zheng-qing...”
    Aufsatz

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

  4. 4
    Clinical sequelae of 17 cases with glycogen storage disease type II/Pompe disease
    Weitere Verfasser: “...Qiu, Zheng-qing...”
    Aufsatz

  5. 5
    Mutation in the SLC37A4 gene of glycogen storage disease type Ib in 15 families of the mainland of China
    Aufsatz

  6. 6
    Mutation analysis and prenatal diagnosis of 2 cases with mucopolysaccharidosis type I
    Weitere Verfasser: “...Qiu, Zheng-Qing...”
    Aufsatz

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

  8. 8
    A brief introduction to the 10th Annual Asian Symposium on lysosomal storage disease
    Aufsatz

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

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

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

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

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