APA

Lahbib S., Leblond C. S., Hamza M., Regnault B., Lemée L., Mathieu A., Jaouadi H., Mkaouar R., Youssef-Turki I. B., Belhadj A., Kraoua I., Bourgeron T. & Abdelhak S. (20190516). Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology. : Journal of applied genetics.

Chicago

Lahbib Saida, Leblond Claire S, Hamza Mariem, Regnault Béatrice, Lemée Laure, Mathieu Alexandre, Jaouadi Hager, Mkaouar Rahma, Youssef-Turki Ilhem Ben, Belhadj Ahlem, Kraoua Ichraf, Bourgeron Thomas and Abdelhak Sonia. 20190516. Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology. : Journal of applied genetics.

Harvard

Lahbib S., Leblond C. S., Hamza M., Regnault B., Lemée L., Mathieu A., Jaouadi H., Mkaouar R., Youssef-Turki I. B., Belhadj A., Kraoua I., Bourgeron T. and Abdelhak S. (20190516). Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology. : Journal of applied genetics.

MLA

Lahbib Saida, Leblond Claire S, Hamza Mariem, Regnault Béatrice, Lemée Laure, Mathieu Alexandre, Jaouadi Hager, Mkaouar Rahma, Youssef-Turki Ilhem Ben, Belhadj Ahlem, Kraoua Ichraf, Bourgeron Thomas and Abdelhak Sonia. Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology. : Journal of applied genetics. 20190516.