Galal, O. M., Rudd, B. T., & Drayer, N. M. (1968). Evaluation of deficiency of 21-hydroxylation in patients with congenital adrenal hyperplasia.
Citação norma ChicagoGalal, O. M., B. T. Rudd, and N. M. Drayer. Evaluation of Deficiency of 21-hydroxylation in Patients With Congenital Adrenal Hyperplasia. 1968.
MLA CitationGalal, O. M., B. T. Rudd, and N. M. Drayer. Evaluation of Deficiency of 21-hydroxylation in Patients With Congenital Adrenal Hyperplasia. 1968.
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