APA citiranje

Vahidi Mehrjardi, M. Y., Maroofian, R., Kalantar, S. M., Jaafarinia, M., Chilton, J., & Dehghani, M. (2017). A Novel Loss-of-Function Mutation in HOXB1 Associated with Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family. Mol Syndromol.

Citação norma Chicago

Vahidi Mehrjardi, Mohammad Yahya, Reza Maroofian, Seyed M. Kalantar, Mojtaba Jaafarinia, John Chilton, and Mohammadreza Dehghani. "A Novel Loss-of-Function Mutation in HOXB1 Associated With Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family." Mol Syndromol 2017.

MLA citiranje

Vahidi Mehrjardi, Mohammad Yahya, et al. "A Novel Loss-of-Function Mutation in HOXB1 Associated With Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family." Mol Syndromol 2017.