Cite
Biochemical diagnosis of a fatal case of Günther's disease in a newborn with hydrops foetalis.
MLA
Verstraeten, L., et al. “Biochemical Diagnosis of a Fatal Case of Günther’s Disease in a Newborn with Hydrops Foetalis.” European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies, vol. 31, no. 3, Mar. 1993, pp. 121–28. EBSCOhost, https://doi.org/10.1515/cclm.1993.31.3.121.
APA
Verstraeten, L., Van Regemorter, N., Pardou, A., de Verneuil, H., Da Silva, V., Rodesch, F., Vermeylen, D., Donner, C., Noël, J. C., Nordmann, Y., & et. al. (1993). Biochemical diagnosis of a fatal case of Günther’s disease in a newborn with hydrops foetalis. European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies, 31(3), 121–128. https://doi.org/10.1515/cclm.1993.31.3.121
Chicago
Verstraeten, L, N Van Regemorter, A Pardou, H de Verneuil, V Da Silva, F Rodesch, D Vermeylen, et al. 1993. “Biochemical Diagnosis of a Fatal Case of Günther’s Disease in a Newborn with Hydrops Foetalis.” European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies 31 (3): 121–28. doi:10.1515/cclm.1993.31.3.121.