Kelsell, D. P., Norgett, E. E., Unsworth, H., Teh, M., Cullup, T., Mein, C. A., . . . O’Toole, E. A. (2005). Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis. The American Society of Human Genetics.
Chicago Style aipamenaKelsell, David P., et al. Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis. The American Society of Human Genetics, 2005.
MLA aipamenaKelsell, David P., et al. Mutations in ABCA12 Underlie the Severe Congenital Skin Disease Harlequin Ichthyosis. The American Society of Human Genetics, 2005.
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