Hội chứng Zellweger (Vietnamese Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hội chứng Zellweger" in Vietnamese language version.

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archive.org

  • Brul, S.; Westerveld, A.; Strijland, A.; Wanders, R.; Schram, A.; Heymans, H.; Schutgens, R.; Van Den Bosch, H.; Tager, J. (tháng 6 năm 1988). “Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis”. Journal of Clinical Investigation (Free full text). 81 (6): 1710–1715. doi:10.1172/JCI113510. PMC 442615. PMID 2454948.

doi.org

  • Brul, S.; Westerveld, A.; Strijland, A.; Wanders, R.; Schram, A.; Heymans, H.; Schutgens, R.; Van Den Bosch, H.; Tager, J. (tháng 6 năm 1988). “Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis”. Journal of Clinical Investigation (Free full text). 81 (6): 1710–1715. doi:10.1172/JCI113510. PMC 442615. PMID 2454948.
  • Wiedemann, H. R. (1991). “Hans-Ulrich Zellweger (1909-1990)”. European Journal of Pediatrics. 150 (7): 451. doi:10.1007/BF01958418. PMID 1915492. S2CID 34905299.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Brul, S.; Westerveld, A.; Strijland, A.; Wanders, R.; Schram, A.; Heymans, H.; Schutgens, R.; Van Den Bosch, H.; Tager, J. (tháng 6 năm 1988). “Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis”. Journal of Clinical Investigation (Free full text). 81 (6): 1710–1715. doi:10.1172/JCI113510. PMC 442615. PMID 2454948.
  • Wiedemann, H. R. (1991). “Hans-Ulrich Zellweger (1909-1990)”. European Journal of Pediatrics. 150 (7): 451. doi:10.1007/BF01958418. PMID 1915492. S2CID 34905299.

ncbi.nlm.nih.gov

  • Brul, S.; Westerveld, A.; Strijland, A.; Wanders, R.; Schram, A.; Heymans, H.; Schutgens, R.; Van Den Bosch, H.; Tager, J. (tháng 6 năm 1988). “Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis”. Journal of Clinical Investigation (Free full text). 81 (6): 1710–1715. doi:10.1172/JCI113510. PMC 442615. PMID 2454948.

semanticscholar.org

api.semanticscholar.org

whonamedit.com