APA

Yalcinkaya C., Erturk O., Tuysuz B., Yesil G., Verbeke J. I. M. L., Keyser B., Stuhrmann M., Steinemann D., Sistermans E. A. & van der Knaap M. S. (20121106). A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?. : Neuropediatrics.

Chicago

Yalcinkaya Cengiz, Erturk Ozdem, Tuysuz Beyhan, Yesil Gozde, Verbeke Jonathan I M L, Keyser Britta, Stuhrmann Manfred, Steinemann Doris, Sistermans Erik A and van der Knaap Marjo S. 20121106. A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?. : Neuropediatrics.

Harvard

Yalcinkaya C., Erturk O., Tuysuz B., Yesil G., Verbeke J. I. M. L., Keyser B., Stuhrmann M., Steinemann D., Sistermans E. A. and van der Knaap M. S. (20121106). A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?. : Neuropediatrics.

MLA

Yalcinkaya Cengiz, Erturk Ozdem, Tuysuz Beyhan, Yesil Gozde, Verbeke Jonathan I M L, Keyser Britta, Stuhrmann Manfred, Steinemann Doris, Sistermans Erik A and van der Knaap Marjo S. A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?. : Neuropediatrics. 20121106.