APA

Hamdan F. F., Myers C. T., Cossette P., Lemay P., Spiegelman D., Laporte A. D., Nassif C., Diallo O., Monlong J., Cadieux-Dion M., Dobrzeniecka S., Meloche C., Retterer K., Cho M. T., Rosenfeld J. A., Bi W., Massicotte C., Miguet M., Brunga L., Regan B. M., Mo K., Tam C., Schneider A., Hollingsworth G., FitzPatrick D. R., Donaldson A., Canham N., Blair E., Kerr B., Fry A. E., Thomas R. H., Shelagh J., Hurst J. A., Brittain H., Blyth M., Lebel R. R., Gerkes E. H., Davis-Keppen L., Stein Q., Chung W. K., Dorison S. J., Benke P. J., Fassi E., Corsten-Janssen N., Kamsteeg E., Mau-Them F. T., Bruel A., Verloes A., Õunap K., Wojcik M. H., Albert D. V. F., Venkateswaran S., Ware T., Jones D., Liu Y., Mohammad S. S., Bizargity P., Bacino C. A., Leuzzi V., Martinelli S., Dallapiccola B., Tartaglia M., Blumkin L., Wierenga K. J., Purcarin G., O'Byrne J. J., Stockler S., Lehman A., Keren B., Nougues M., Mignot C., Auvin S., Nava C., Hiatt S. M., Bebin M., Shao Y., Scaglia F., Lalani S. R., Frye R. E., Jarjour I. T., Jacques S., Boucher R., Riou E., Srour M., Carmant L., Lortie A., Major P., Diadori P., Dubeau F., D'Anjou G., Bourque G., Berkovic S. F., Sadleir L. G., Campeau P. M., Kibar Z., Lafrenière R. G., Girard S. L., Mercimek-Mahmutoglu S., Boelman C., Rouleau G. A., Scheffer I. E., Mefford H. C., Andrade D. M., Rossignol E., Minassian B. A. & Michaud J. L. (20171113). High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. : American journal of human genetics.

Chicago

Hamdan Fadi F, Myers Candace T, Cossette Patrick, Lemay Philippe, Spiegelman Dan, Laporte Alexandre Dionne, Nassif Christina, Diallo Ousmane, Monlong Jean, Cadieux-Dion Maxime, Dobrzeniecka Sylvia, Meloche Caroline, Retterer Kyle, Cho Megan T, Rosenfeld Jill A, Bi Weimin, Massicotte Christine, Miguet Marguerite, Brunga Ledia, Regan Brigid M, Mo Kelly, Tam Cory, Schneider Amy, Hollingsworth Georgie, FitzPatrick David R, Donaldson Alan, Canham Natalie, Blair Edward, Kerr Bronwyn, Fry Andrew E, Thomas Rhys H, Shelagh Joss, Hurst Jane A, Brittain Helen, Blyth Moira, Lebel Robert Roger, Gerkes Erica H, Davis-Keppen Laura, Stein Quinn, Chung Wendy K, Dorison Sara J, Benke Paul J, Fassi Emily, Corsten-Janssen Nicole, Kamsteeg Erik-Jan, Mau-Them Frederic T, Bruel Ange-Line, Verloes Alain, Õunap Katrin, Wojcik Monica H, Albert Dara V F, Venkateswaran Sunita, Ware Tyson, Jones Dean, Liu Yu-Chi, Mohammad Shekeeb S, Bizargity Peyman, Bacino Carlos A, Leuzzi Vincenzo, Martinelli Simone, Dallapiccola Bruno, Tartaglia Marco, Blumkin Lubov, Wierenga Klaas J, Purcarin Gabriela, O'Byrne James J, Stockler Sylvia, Lehman Anna, Keren Boris, Nougues Marie-Christine, Mignot Cyril, Auvin Stéphane, Nava Caroline, Hiatt Susan M, Bebin Martina, Shao Yunru, Scaglia Fernando, Lalani Seema R, Frye Richard E, Jarjour Imad T, Jacques Stéphanie, Boucher Renee-Myriam, Riou Emilie, Srour Myriam, Carmant Lionel, Lortie Anne, Major Philippe, Diadori Paola, Dubeau François, D'Anjou Guy, Bourque Guillaume, Berkovic Samuel F, Sadleir Lynette G, Campeau Philippe M, Kibar Zoha, Lafrenière Ronald G, Girard Simon L, Mercimek-Mahmutoglu Saadet, Boelman Cyrus, Rouleau Guy A, Scheffer Ingrid E, Mefford Heather C, Andrade Danielle M, Rossignol Elsa, Minassian Berge A and Michaud Jacques L. 20171113. High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. : American journal of human genetics.

Harvard

Hamdan F. F., Myers C. T., Cossette P., Lemay P., Spiegelman D., Laporte A. D., Nassif C., Diallo O., Monlong J., Cadieux-Dion M., Dobrzeniecka S., Meloche C., Retterer K., Cho M. T., Rosenfeld J. A., Bi W., Massicotte C., Miguet M., Brunga L., Regan B. M., Mo K., Tam C., Schneider A., Hollingsworth G., FitzPatrick D. R., Donaldson A., Canham N., Blair E., Kerr B., Fry A. E., Thomas R. H., Shelagh J., Hurst J. A., Brittain H., Blyth M., Lebel R. R., Gerkes E. H., Davis-Keppen L., Stein Q., Chung W. K., Dorison S. J., Benke P. J., Fassi E., Corsten-Janssen N., Kamsteeg E., Mau-Them F. T., Bruel A., Verloes A., Õunap K., Wojcik M. H., Albert D. V. F., Venkateswaran S., Ware T., Jones D., Liu Y., Mohammad S. S., Bizargity P., Bacino C. A., Leuzzi V., Martinelli S., Dallapiccola B., Tartaglia M., Blumkin L., Wierenga K. J., Purcarin G., O'Byrne J. J., Stockler S., Lehman A., Keren B., Nougues M., Mignot C., Auvin S., Nava C., Hiatt S. M., Bebin M., Shao Y., Scaglia F., Lalani S. R., Frye R. E., Jarjour I. T., Jacques S., Boucher R., Riou E., Srour M., Carmant L., Lortie A., Major P., Diadori P., Dubeau F., D'Anjou G., Bourque G., Berkovic S. F., Sadleir L. G., Campeau P. M., Kibar Z., Lafrenière R. G., Girard S. L., Mercimek-Mahmutoglu S., Boelman C., Rouleau G. A., Scheffer I. E., Mefford H. C., Andrade D. M., Rossignol E., Minassian B. A. and Michaud J. L. (20171113). High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. : American journal of human genetics.

MLA

Hamdan Fadi F, Myers Candace T, Cossette Patrick, Lemay Philippe, Spiegelman Dan, Laporte Alexandre Dionne, Nassif Christina, Diallo Ousmane, Monlong Jean, Cadieux-Dion Maxime, Dobrzeniecka Sylvia, Meloche Caroline, Retterer Kyle, Cho Megan T, Rosenfeld Jill A, Bi Weimin, Massicotte Christine, Miguet Marguerite, Brunga Ledia, Regan Brigid M, Mo Kelly, Tam Cory, Schneider Amy, Hollingsworth Georgie, FitzPatrick David R, Donaldson Alan, Canham Natalie, Blair Edward, Kerr Bronwyn, Fry Andrew E, Thomas Rhys H, Shelagh Joss, Hurst Jane A, Brittain Helen, Blyth Moira, Lebel Robert Roger, Gerkes Erica H, Davis-Keppen Laura, Stein Quinn, Chung Wendy K, Dorison Sara J, Benke Paul J, Fassi Emily, Corsten-Janssen Nicole, Kamsteeg Erik-Jan, Mau-Them Frederic T, Bruel Ange-Line, Verloes Alain, Õunap Katrin, Wojcik Monica H, Albert Dara V F, Venkateswaran Sunita, Ware Tyson, Jones Dean, Liu Yu-Chi, Mohammad Shekeeb S, Bizargity Peyman, Bacino Carlos A, Leuzzi Vincenzo, Martinelli Simone, Dallapiccola Bruno, Tartaglia Marco, Blumkin Lubov, Wierenga Klaas J, Purcarin Gabriela, O'Byrne James J, Stockler Sylvia, Lehman Anna, Keren Boris, Nougues Marie-Christine, Mignot Cyril, Auvin Stéphane, Nava Caroline, Hiatt Susan M, Bebin Martina, Shao Yunru, Scaglia Fernando, Lalani Seema R, Frye Richard E, Jarjour Imad T, Jacques Stéphanie, Boucher Renee-Myriam, Riou Emilie, Srour Myriam, Carmant Lionel, Lortie Anne, Major Philippe, Diadori Paola, Dubeau François, D'Anjou Guy, Bourque Guillaume, Berkovic Samuel F, Sadleir Lynette G, Campeau Philippe M, Kibar Zoha, Lafrenière Ronald G, Girard Simon L, Mercimek-Mahmutoglu Saadet, Boelman Cyrus, Rouleau Guy A, Scheffer Ingrid E, Mefford Heather C, Andrade Danielle M, Rossignol Elsa, Minassian Berge A and Michaud Jacques L. High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. : American journal of human genetics. 20171113.