Burkitt Wright, E. M. M., Porter, L. F., Spencer, H. L., Clayton-Smith, J., Au, L., Munier, F. L., . . . Black, G. C. M. (2013). Brittle cornea syndrome: Recognition, molecular diagnosis and management. Orphanet Journal of Rare Diseases, 8(1), 1. https://doi.org/10.1186/1750-1172-8-68
Chicago Style (17th ed.) CitationBurkitt Wright, Emma M. M., et al. "Brittle Cornea Syndrome: Recognition, Molecular Diagnosis and Management." Orphanet Journal of Rare Diseases 8, no. 1 (2013): 1. https://doi.org/10.1186/1750-1172-8-68.
MLA (9th ed.) CitationBurkitt Wright, Emma M. M., et al. "Brittle Cornea Syndrome: Recognition, Molecular Diagnosis and Management." Orphanet Journal of Rare Diseases, vol. 8, no. 1, 2013, p. 1, https://doi.org/10.1186/1750-1172-8-68.