APA

Cavallin M., Bijlsma E. K., El Morjani A., Moutton S., Peeters E. A. J., Maillard C., Pedespan J. M., Guerrot A., Drouin-Garaud V., Coubes C., Genevieve D., Bole-Feysot C., Fourrage C., Steffann J. & Bahi-Buisson N. (20180221). Recurrent KIF2A mutations are responsible for classic lissencephaly. : Neurogenetics.

Chicago

Cavallin Mara, Bijlsma Emilia K, El Morjani Adrienne, Moutton Sébastien, Peeters Els A J, Maillard Camille, Pedespan Jean Michel, Guerrot Anne-Marie, Drouin-Garaud Valérie, Coubes Christine, Genevieve David, Bole-Feysot Christine, Fourrage Cecile, Steffann Julie and Bahi-Buisson Nadia. 20180221. Recurrent KIF2A mutations are responsible for classic lissencephaly. : Neurogenetics.

Harvard

Cavallin M., Bijlsma E. K., El Morjani A., Moutton S., Peeters E. A. J., Maillard C., Pedespan J. M., Guerrot A., Drouin-Garaud V., Coubes C., Genevieve D., Bole-Feysot C., Fourrage C., Steffann J. and Bahi-Buisson N. (20180221). Recurrent KIF2A mutations are responsible for classic lissencephaly. : Neurogenetics.

MLA

Cavallin Mara, Bijlsma Emilia K, El Morjani Adrienne, Moutton Sébastien, Peeters Els A J, Maillard Camille, Pedespan Jean Michel, Guerrot Anne-Marie, Drouin-Garaud Valérie, Coubes Christine, Genevieve David, Bole-Feysot Christine, Fourrage Cecile, Steffann Julie and Bahi-Buisson Nadia. Recurrent KIF2A mutations are responsible for classic lissencephaly. : Neurogenetics. 20180221.