APA

Pebrel-Richard C., Rouzade C., Kemeny S., Eymard-Pierre E., Gay-Bellile M., Gouas L., Tchirkov A., Goumy C. & Vago P. (20160516). Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay. : American journal of medical genetics. Part A.

Chicago

Pebrel-Richard Celine, Rouzade Charles, Kemeny Stephan, Eymard-Pierre Eleonore, Gay-Bellile Mathilde, Gouas Laetitia, Tchirkov Andreï, Goumy Carole and Vago Philippe. 20160516. Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay. : American journal of medical genetics. Part A.

Harvard

Pebrel-Richard C., Rouzade C., Kemeny S., Eymard-Pierre E., Gay-Bellile M., Gouas L., Tchirkov A., Goumy C. and Vago P. (20160516). Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay. : American journal of medical genetics. Part A.

MLA

Pebrel-Richard Celine, Rouzade Charles, Kemeny Stephan, Eymard-Pierre Eleonore, Gay-Bellile Mathilde, Gouas Laetitia, Tchirkov Andreï, Goumy Carole and Vago Philippe. Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay. : American journal of medical genetics. Part A. 20160516.