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. Elsevier.
Citação norma ChicagoTwigg, Stephen R.F., et al. Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated With Defective Lateralization. Elsevier, 2012.
ציטוט MLATwigg, Stephen R.F., et al. Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated With Defective Lateralization. Elsevier, 2012.
אזהרה: ציטוטים אלה לעיתים לא מדויקים ב 100%.