APA
Marelli C., Guissart C., Hubsch C., Renaud M., Villemin J., Larrieu L., Charles P., Ayrignac X., Sacconi S., Collignon P., Cuntz-Shadfar D., Perrin L., Benarrosh A., Degardin A., Lagha-Boukbiza O., Mutez E., Carlander B., Morales R. J., Gonzalez V., Carra-Dalliere C., Azakri S., Mignard C., Ollagnon E., Pageot N., Chretien D., Geny C., Azulay J., Tranchant C., Claustres M., Labauge P., Anheim M., Goizet C., Calvas P. & Koenig M. (20171107). Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias. : Human mutation.
Chicago
Marelli Cecilia, Guissart Claire, Hubsch Cecile, Renaud Mathilde, Villemin Jean-Philippe, Larrieu Lise, Charles Perrine, Ayrignac Xavier, Sacconi Sabrina, Collignon Patrick, Cuntz-Shadfar Danielle, Perrin Laurine, Benarrosh Anelia, Degardin Adrian, Lagha-Boukbiza Ouhaïd, Mutez Eugenie, Carlander Bertrand, Morales Raul Juntas, Gonzalez Victoria, Carra-Dalliere Clarisse, Azakri Souhayla, Mignard Claude, Ollagnon Elisabeth, Pageot Nicolas, Chretien Dominique, Geny Christian, Azulay Jean-Philippe, Tranchant Christine, Claustres Mireille, Labauge Pierre, Anheim Mathieu, Goizet Cyril, Calvas Patrick and Koenig Michel. 20171107. Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias. : Human mutation.
Harvard
Marelli C., Guissart C., Hubsch C., Renaud M., Villemin J., Larrieu L., Charles P., Ayrignac X., Sacconi S., Collignon P., Cuntz-Shadfar D., Perrin L., Benarrosh A., Degardin A., Lagha-Boukbiza O., Mutez E., Carlander B., Morales R. J., Gonzalez V., Carra-Dalliere C., Azakri S., Mignard C., Ollagnon E., Pageot N., Chretien D., Geny C., Azulay J., Tranchant C., Claustres M., Labauge P., Anheim M., Goizet C., Calvas P. and Koenig M. (20171107). Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias. : Human mutation.
MLA
Marelli Cecilia, Guissart Claire, Hubsch Cecile, Renaud Mathilde, Villemin Jean-Philippe, Larrieu Lise, Charles Perrine, Ayrignac Xavier, Sacconi Sabrina, Collignon Patrick, Cuntz-Shadfar Danielle, Perrin Laurine, Benarrosh Anelia, Degardin Adrian, Lagha-Boukbiza Ouhaïd, Mutez Eugenie, Carlander Bertrand, Morales Raul Juntas, Gonzalez Victoria, Carra-Dalliere Clarisse, Azakri Souhayla, Mignard Claude, Ollagnon Elisabeth, Pageot Nicolas, Chretien Dominique, Geny Christian, Azulay Jean-Philippe, Tranchant Christine, Claustres Mireille, Labauge Pierre, Anheim Mathieu, Goizet Cyril, Calvas Patrick and Koenig Michel. Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias. : Human mutation. 20171107.