APA

Hamdan F. F., Daoud H., Rochefort D., Piton A., Gauthier J., Langlois M., Foomani G., Dobrzeniecka S., Krebs M., Joober R., Lafrenière R. G., Lacaille J., Mottron L., Drapeau P., Beauchamp M. H., Phillips M. S., Fombonne E., Rouleau G. A. & Michaud J. L. (20110124). De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. : American journal of human genetics.

Chicago

Hamdan Fadi F, Daoud Hussein, Rochefort Daniel, Piton Amélie, Gauthier Julie, Langlois Mathieu, Foomani Gila, Dobrzeniecka Sylvia, Krebs Marie-Odile, Joober Ridha, Lafrenière Ronald G, Lacaille Jean-Claude, Mottron Laurent, Drapeau Pierre, Beauchamp Miriam H, Phillips Michael S, Fombonne Eric, Rouleau Guy A and Michaud Jacques L. 20110124. De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. : American journal of human genetics.

Harvard

Hamdan F. F., Daoud H., Rochefort D., Piton A., Gauthier J., Langlois M., Foomani G., Dobrzeniecka S., Krebs M., Joober R., Lafrenière R. G., Lacaille J., Mottron L., Drapeau P., Beauchamp M. H., Phillips M. S., Fombonne E., Rouleau G. A. and Michaud J. L. (20110124). De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. : American journal of human genetics.

MLA

Hamdan Fadi F, Daoud Hussein, Rochefort Daniel, Piton Amélie, Gauthier Julie, Langlois Mathieu, Foomani Gila, Dobrzeniecka Sylvia, Krebs Marie-Odile, Joober Ridha, Lafrenière Ronald G, Lacaille Jean-Claude, Mottron Laurent, Drapeau Pierre, Beauchamp Miriam H, Phillips Michael S, Fombonne Eric, Rouleau Guy A and Michaud Jacques L. De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. : American journal of human genetics. 20110124.