APA

Pacault M., Vincent M., Besnard T., Kannengiesser C., Bénéteau C., Barbarot S., Latypova X., Belabbas K., Lamazière A., Winer N., Joubert M., Bézieau S., Isidor B., Mercier S., Nizon M., Leclerc-Mercier S., Hadj-Rabia S. & Dufernez F. (20190328). New splicing pathogenic variant in EBP causing extreme familial variability of Conradi-Hünermann-Happle Syndrome. : European journal of human genetics : EJHG.

Chicago

Pacault Mathilde, Vincent Marie, Besnard Thomas, Kannengiesser Caroline, Bénéteau Claire, Barbarot Sébastien, Latypova Xénia, Belabbas Khaldia, Lamazière Antonin, Winer Norbert, Joubert Madeleine, Bézieau Stéphane, Isidor Bertrand, Mercier Sandra, Nizon Mathilde, Leclerc-Mercier Stéphanie, Hadj-Rabia Smail and Dufernez Fabienne. 20190328. New splicing pathogenic variant in EBP causing extreme familial variability of Conradi-Hünermann-Happle Syndrome. : European journal of human genetics : EJHG.

Harvard

Pacault M., Vincent M., Besnard T., Kannengiesser C., Bénéteau C., Barbarot S., Latypova X., Belabbas K., Lamazière A., Winer N., Joubert M., Bézieau S., Isidor B., Mercier S., Nizon M., Leclerc-Mercier S., Hadj-Rabia S. and Dufernez F. (20190328). New splicing pathogenic variant in EBP causing extreme familial variability of Conradi-Hünermann-Happle Syndrome. : European journal of human genetics : EJHG.

MLA

Pacault Mathilde, Vincent Marie, Besnard Thomas, Kannengiesser Caroline, Bénéteau Claire, Barbarot Sébastien, Latypova Xénia, Belabbas Khaldia, Lamazière Antonin, Winer Norbert, Joubert Madeleine, Bézieau Stéphane, Isidor Bertrand, Mercier Sandra, Nizon Mathilde, Leclerc-Mercier Stéphanie, Hadj-Rabia Smail and Dufernez Fabienne. New splicing pathogenic variant in EBP causing extreme familial variability of Conradi-Hünermann-Happle Syndrome. : European journal of human genetics : EJHG. 20190328.