APA

Goumy C., Gay-Bellile M., Salaun G., Kemeny S., Eymard-Pierre E., Biard M., Pebrel-Richard C., Vanlieferinghen P., Francannet C., Tchirkov A., Laurichesse H., Rouzade C., Gouas L. & Vago P. (20171016). A novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardation. : Birth defects research. Part A, Clinical and molecular teratology.

Chicago

Goumy Carole, Gay-Bellile Mathilde, Salaun Gaelle, Kemeny Stephan, Eymard-Pierre Eleonore, Biard Marie, Pebrel-Richard Celine, Vanlieferinghen Philippe, Francannet Christine, Tchirkov Andrei, Laurichesse Helene, Rouzade Charles, Gouas Laetitia and Vago Philippe. 20171016. A novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardation. : Birth defects research. Part A, Clinical and molecular teratology.

Harvard

Goumy C., Gay-Bellile M., Salaun G., Kemeny S., Eymard-Pierre E., Biard M., Pebrel-Richard C., Vanlieferinghen P., Francannet C., Tchirkov A., Laurichesse H., Rouzade C., Gouas L. and Vago P. (20171016). A novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardation. : Birth defects research. Part A, Clinical and molecular teratology.

MLA

Goumy Carole, Gay-Bellile Mathilde, Salaun Gaelle, Kemeny Stephan, Eymard-Pierre Eleonore, Biard Marie, Pebrel-Richard Celine, Vanlieferinghen Philippe, Francannet Christine, Tchirkov Andrei, Laurichesse Helene, Rouzade Charles, Gouas Laetitia and Vago Philippe. A novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardation. : Birth defects research. Part A, Clinical and molecular teratology. 20171016.