APA
Miguet M., Thevenon J., Laugel V., Lefebvre M., Bourchany A., Rivière J., Duffourd Y., Schaefer E., Antal M. C., Abida R., Weingertner A., Kremer V., Vabres P., Morice-Picard F., Gonzales M., Lipsker D., Fraitag S., Mandel J., Chelly J., Dollfus H., Faivre L., Thauvin-Robinet C., Calmels N. & El Chehadeh S. (20170726). Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features. : Prenatal diagnosis.
Chicago
Miguet Marguerite, Thevenon Julien, Laugel Vincent, Lefebvre Mathilde, Bourchany Aurélie, Rivière Jean-Baptiste, Duffourd Yannis, Schaefer Elise, Antal Maria Cristina, Abida Rosalie, Weingertner Anne-Sophie, Kremer Valérie, Vabres Pierre, Morice-Picard Fanny, Gonzales Marie, Lipsker Dan, Fraitag Sylvie, Mandel Jean-Louis, Chelly Jamel, Dollfus Hélène, Faivre Laurence, Thauvin-Robinet Christel, Calmels Nadège and El Chehadeh Salima. 20170726. Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features. : Prenatal diagnosis.
Harvard
Miguet M., Thevenon J., Laugel V., Lefebvre M., Bourchany A., Rivière J., Duffourd Y., Schaefer E., Antal M. C., Abida R., Weingertner A., Kremer V., Vabres P., Morice-Picard F., Gonzales M., Lipsker D., Fraitag S., Mandel J., Chelly J., Dollfus H., Faivre L., Thauvin-Robinet C., Calmels N. and El Chehadeh S. (20170726). Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features. : Prenatal diagnosis.
MLA
Miguet Marguerite, Thevenon Julien, Laugel Vincent, Lefebvre Mathilde, Bourchany Aurélie, Rivière Jean-Baptiste, Duffourd Yannis, Schaefer Elise, Antal Maria Cristina, Abida Rosalie, Weingertner Anne-Sophie, Kremer Valérie, Vabres Pierre, Morice-Picard Fanny, Gonzales Marie, Lipsker Dan, Fraitag Sylvie, Mandel Jean-Louis, Chelly Jamel, Dollfus Hélène, Faivre Laurence, Thauvin-Robinet Christel, Calmels Nadège and El Chehadeh Salima. Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features. : Prenatal diagnosis. 20170726.