Anderson-Cohen, M., Holland, S. M., Kuhns, D. B., Fleisher, T. A., Ding, L., Brenner, S., . . . Roesler, J. (2003). Severe phenotype of chronic granulomatous disease presenting in a female with a de novo mutation in gp91-phox and a non familial, extremely skewed X chromosome inactivation. Clinical immunology (Orlando, Fla.), 109(3), 308.
Style de citation ChicagoAnderson-Cohen, Mindy, Steve M. Holland, Doug B. Kuhns, Thomas A. Fleisher, Li Ding, Sebastian Brenner, Harry L. Malech, et Joachim Roesler. "Severe Phenotype of Chronic Granulomatous Disease Presenting in a Female with a De Novo Mutation in Gp91-phox and a Non Familial, Extremely Skewed X Chromosome Inactivation." Clinical Immunology (Orlando, Fla.) 109, no. 3 (2003): 308.
Style de citation MLAAnderson-Cohen, Mindy, et al. "Severe Phenotype of Chronic Granulomatous Disease Presenting in a Female with a De Novo Mutation in Gp91-phox and a Non Familial, Extremely Skewed X Chromosome Inactivation." Clinical Immunology (Orlando, Fla.), vol. 109, no. 3, 2003, p. 308.