APA
Poirier K., Lebrun N., Broix L., Tian G., Saillour Y., Boscheron C., Parrini E., Valence S., Pierre B. S., Oger M., Lacombe D., Geneviève D., Fontana E., Darra F., Cances C., Barth M., Bonneau D., Bernadina B. D., N'guyen S., Gitiaux C., Parent P., des Portes V., Pedespan J. M., Legrez V., Castelnau-Ptakine L., Nitschke P., Hieu T., Masson C., Zelenika D., Andrieux A., Francis F., Guerrini R., Cowan N. J., Bahi-Buisson N. & Chelly J. (20130802). Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. : Nature genetics.
Chicago
Poirier Karine, Lebrun Nicolas, Broix Loic, Tian Guoling, Saillour Yoann, Boscheron Cécile, Parrini Elena, Valence Stephanie, Pierre Benjamin Saint, Oger Madison, Lacombe Didier, Geneviève David, Fontana Elena, Darra Franscesca, Cances Claude, Barth Magalie, Bonneau Dominique, Bernadina Bernardo Dalla, N'guyen Sylvie, Gitiaux Cyril, Parent Philippe, des Portes Vincent, Pedespan Jean Michel, Legrez Victoire, Castelnau-Ptakine Laetitia, Nitschke Patrick, Hieu Thierry, Masson Cecile, Zelenika Diana, Andrieux Annie, Francis Fiona, Guerrini Renzo, Cowan Nicholas J, Bahi-Buisson Nadia and Chelly Jamel. 20130802. Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. : Nature genetics.
Harvard
Poirier K., Lebrun N., Broix L., Tian G., Saillour Y., Boscheron C., Parrini E., Valence S., Pierre B. S., Oger M., Lacombe D., Geneviève D., Fontana E., Darra F., Cances C., Barth M., Bonneau D., Bernadina B. D., N'guyen S., Gitiaux C., Parent P., des Portes V., Pedespan J. M., Legrez V., Castelnau-Ptakine L., Nitschke P., Hieu T., Masson C., Zelenika D., Andrieux A., Francis F., Guerrini R., Cowan N. J., Bahi-Buisson N. and Chelly J. (20130802). Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. : Nature genetics.
MLA
Poirier Karine, Lebrun Nicolas, Broix Loic, Tian Guoling, Saillour Yoann, Boscheron Cécile, Parrini Elena, Valence Stephanie, Pierre Benjamin Saint, Oger Madison, Lacombe Didier, Geneviève David, Fontana Elena, Darra Franscesca, Cances Claude, Barth Magalie, Bonneau Dominique, Bernadina Bernardo Dalla, N'guyen Sylvie, Gitiaux Cyril, Parent Philippe, des Portes Vincent, Pedespan Jean Michel, Legrez Victoire, Castelnau-Ptakine Laetitia, Nitschke Patrick, Hieu Thierry, Masson Cecile, Zelenika Diana, Andrieux Annie, Francis Fiona, Guerrini Renzo, Cowan Nicholas J, Bahi-Buisson Nadia and Chelly Jamel. Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. : Nature genetics. 20130802.