Coinheritance of two rare genodermatoses (Papillon–Lefèvre syndrome and oculocutaneous albinism type 1) in two families: a genetic study.

MLA

Hewitt, C., et al. “Coinheritance of Two Rare Genodermatoses (Papillon–Lefèvre Syndrome and Oculocutaneous Albinism Type 1) in Two Families: A Genetic Study.” British Journal of Dermatology, vol. 151, no. 6, Dec. 2004, pp. 1261–65. EBSCOhost, https://doi.org/10.1111/j.1365-2133.2004.06237.x.

APA

Hewitt, C., Wu, C.-L., Hattab, F. N., Amin, W., Ghaffar, K. A., Toomes, C., Sloan, P., Read, A. P., James, J. A., & Thakker, N. S. (2004). Coinheritance of two rare genodermatoses (Papillon–Lefèvre syndrome and oculocutaneous albinism type 1) in two families: a genetic study. British Journal of Dermatology, 151(6), 1261–1265. https://doi.org/10.1111/j.1365-2133.2004.06237.x

Chicago

Hewitt, C., C. -L. Wu, F. N. Hattab, W. Amin, K. A. Ghaffar, C. Toomes, P. Sloan, A. P. Read, J. A. James, and N. S. Thakker. 2004. “Coinheritance of Two Rare Genodermatoses (Papillon–Lefèvre Syndrome and Oculocutaneous Albinism Type 1) in Two Families: A Genetic Study.” British Journal of Dermatology 151 (6): 1261–65. doi:10.1111/j.1365-2133.2004.06237.x.