Congenital disorder of glycosylation type Id: clinical phenotype, molecular analysis, prenatal diagnosis, and glycosylation of fetal proteins.

MLA

Denecke, Jonas, et al. “Congenital Disorder of Glycosylation Type Id: Clinical Phenotype, Molecular Analysis, Prenatal Diagnosis, and Glycosylation of Fetal Proteins.” Pediatric Research, vol. 58, no. 2, Aug. 2005, pp. 248–53. EBSCOhost, https://doi.org/10.1203/01.PDR.0000169963.94378.B6.

APA

Denecke, J., Kranz, C., von Kleist-Retzow, J. C., Bosse, K., Herkenrath, P., Debus, O., Harms, E., & Marquardt, T. (2005). Congenital disorder of glycosylation type Id: clinical phenotype, molecular analysis, prenatal diagnosis, and glycosylation of fetal proteins. Pediatric Research, 58(2), 248–253. https://doi.org/10.1203/01.PDR.0000169963.94378.B6

Chicago

Denecke, Jonas, Christian Kranz, Juergen Ch von Kleist-Retzow, Kristin Bosse, Peter Herkenrath, Otfried Debus, Erik Harms, and Thorsten Marquardt. 2005. “Congenital Disorder of Glycosylation Type Id: Clinical Phenotype, Molecular Analysis, Prenatal Diagnosis, and Glycosylation of Fetal Proteins.” Pediatric Research 58 (2): 248–53. doi:10.1203/01.PDR.0000169963.94378.B6.