APA
Létard P., Drunat S., Vial Y., Duerinckx S., Ernault A., Amram D., Arpin S., Bertoli M., Busa T., Ceulemans B., Desir J., Doco-Fenzy M., Elalaoui S. C., Devriendt K., Faivre L., Francannet C., Geneviève D., Gérard M., Gitiaux C., Julia S., Lebon S., Lubala T., Mathieu-Dramard M., Maurey H., Metreau J., Nasserereddine S., Nizon M., Pierquin G., Pouvreau N., Rivier-Ringenbach C., Rossi M., Schaefer E., Sefiani A., Sigaudy S., Sznajer Y., Tunca Y., Guilmin Crepon S., Alberti C., Elmaleh-Bergès M., Benzacken B., Wollnick B., Woods C. G., Rauch A., Abramowicz M., El Ghouzzi V., Gressens P., Verloes A. & Passemard S. (20190328). Autosomal recessive primary microcephaly due to ASPM mutations: An update. : Human mutation.
Chicago
Létard Pascaline, Drunat Séverine, Vial Yoann, Duerinckx Sarah, Ernault Anais, Amram Daniel, Arpin Stéphanie, Bertoli Marta, Busa Tiffany, Ceulemans Berten, Desir Julie, Doco-Fenzy Martine, Elalaoui Siham Chafai, Devriendt Koenraad, Faivre Laurence, Francannet Christine, Geneviève David, Gérard Marion, Gitiaux Cyril, Julia Sophie, Lebon Sébastien, Lubala Toni, Mathieu-Dramard Michèle, Maurey Hélène, Metreau Julia, Nasserereddine Sanaa, Nizon Mathilde, Pierquin Geneviève, Pouvreau Nathalie, Rivier-Ringenbach Clothilde, Rossi Massimiliano, Schaefer Elise, Sefiani Abdelaziz, Sigaudy Sabine, Sznajer Yves, Tunca Yusuf, Guilmin Crepon Sophie, Alberti Corinne, Elmaleh-Bergès Monique, Benzacken Brigitte, Wollnick Bernd, Woods C Geoffrey, Rauch Anita, Abramowicz Marc, El Ghouzzi Vincent, Gressens Pierre, Verloes Alain and Passemard Sandrine. 20190328. Autosomal recessive primary microcephaly due to ASPM mutations: An update. : Human mutation.
Harvard
Létard P., Drunat S., Vial Y., Duerinckx S., Ernault A., Amram D., Arpin S., Bertoli M., Busa T., Ceulemans B., Desir J., Doco-Fenzy M., Elalaoui S. C., Devriendt K., Faivre L., Francannet C., Geneviève D., Gérard M., Gitiaux C., Julia S., Lebon S., Lubala T., Mathieu-Dramard M., Maurey H., Metreau J., Nasserereddine S., Nizon M., Pierquin G., Pouvreau N., Rivier-Ringenbach C., Rossi M., Schaefer E., Sefiani A., Sigaudy S., Sznajer Y., Tunca Y., Guilmin Crepon S., Alberti C., Elmaleh-Bergès M., Benzacken B., Wollnick B., Woods C. G., Rauch A., Abramowicz M., El Ghouzzi V., Gressens P., Verloes A. and Passemard S. (20190328). Autosomal recessive primary microcephaly due to ASPM mutations: An update. : Human mutation.
MLA
Létard Pascaline, Drunat Séverine, Vial Yoann, Duerinckx Sarah, Ernault Anais, Amram Daniel, Arpin Stéphanie, Bertoli Marta, Busa Tiffany, Ceulemans Berten, Desir Julie, Doco-Fenzy Martine, Elalaoui Siham Chafai, Devriendt Koenraad, Faivre Laurence, Francannet Christine, Geneviève David, Gérard Marion, Gitiaux Cyril, Julia Sophie, Lebon Sébastien, Lubala Toni, Mathieu-Dramard Michèle, Maurey Hélène, Metreau Julia, Nasserereddine Sanaa, Nizon Mathilde, Pierquin Geneviève, Pouvreau Nathalie, Rivier-Ringenbach Clothilde, Rossi Massimiliano, Schaefer Elise, Sefiani Abdelaziz, Sigaudy Sabine, Sznajer Yves, Tunca Yusuf, Guilmin Crepon Sophie, Alberti Corinne, Elmaleh-Bergès Monique, Benzacken Brigitte, Wollnick Bernd, Woods C Geoffrey, Rauch Anita, Abramowicz Marc, El Ghouzzi Vincent, Gressens Pierre, Verloes Alain and Passemard Sandrine. Autosomal recessive primary microcephaly due to ASPM mutations: An update. : Human mutation. 20190328.