APA ציטוט

Vuillaumier-Barro..., S., Hetet, G., Barnier, A., Dupre, T., Cuer, M., de Lonlay, P., . . . Seta, N. (2000). Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients. BMJ Group.

Citação norma Chicago

Vuillaumier-Barro..., S., et al. Identification of Four Novel PMM2 Mutations in Congenital Disorders of Glycosylation (CDG) Ia French Patients. BMJ Group, 2000.

ציטוט MLA

Vuillaumier-Barro..., S., et al. Identification of Four Novel PMM2 Mutations in Congenital Disorders of Glycosylation (CDG) Ia French Patients. BMJ Group, 2000.