APA
Muller J., Stoetzel C., Vincent M. C., Leitch C. C., Laurier V., Danse J. M., Hellé S., Marion V., Bennouna-Greene V., Vicaire S., Megarbane A., Kaplan J., Drouin-Garraud V., Hamdani M., Sigaudy S., Francannet C., Roume J., Bitoun P., Goldenberg A., Philip N., Odent S., Green J., Cossée M., Davis E. E., Katsanis N., Bonneau D., Verloes A., Poch O., Mandel J. L. & Dollfus H. (20100428). Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease. : Human genetics.
Chicago
Muller Jean, Stoetzel C, Vincent M C, Leitch C C, Laurier V, Danse J M, Hellé S, Marion V, Bennouna-Greene V, Vicaire S, Megarbane A, Kaplan J, Drouin-Garraud V, Hamdani M, Sigaudy S, Francannet C, Roume J, Bitoun P, Goldenberg A, Philip N, Odent S, Green J, Cossée M, Davis E E, Katsanis N, Bonneau D, Verloes A, Poch O, Mandel J L and Dollfus H. 20100428. Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease. : Human genetics.
Harvard
Muller J., Stoetzel C., Vincent M. C., Leitch C. C., Laurier V., Danse J. M., Hellé S., Marion V., Bennouna-Greene V., Vicaire S., Megarbane A., Kaplan J., Drouin-Garraud V., Hamdani M., Sigaudy S., Francannet C., Roume J., Bitoun P., Goldenberg A., Philip N., Odent S., Green J., Cossée M., Davis E. E., Katsanis N., Bonneau D., Verloes A., Poch O., Mandel J. L. and Dollfus H. (20100428). Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease. : Human genetics.
MLA
Muller Jean, Stoetzel C, Vincent M C, Leitch C C, Laurier V, Danse J M, Hellé S, Marion V, Bennouna-Greene V, Vicaire S, Megarbane A, Kaplan J, Drouin-Garraud V, Hamdani M, Sigaudy S, Francannet C, Roume J, Bitoun P, Goldenberg A, Philip N, Odent S, Green J, Cossée M, Davis E E, Katsanis N, Bonneau D, Verloes A, Poch O, Mandel J L and Dollfus H. Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease. : Human genetics. 20100428.