Twigg, S., Lloyd, D., Jenkins, D., Elçioglu, N., Cooper, C., Al-Sannaa, N., . . . Wilkie, A. (2012). Mutations in multidomain protein MEGF8 identify a carpenter syndrome subtype associated with defective lateralization.
Chicago Style (17. basım) AtıfTwigg, S., et al. Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization. 2012.
MLA (9th ed.) AtıfTwigg, S., et al. Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization. 2012.
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