APA

Natera-De Benito D., Vidal-Esteban A., Sanchez-Del Pozo J., Moreno-Garcia M., Suela-Rubio J., Cruz-Rojo J. & Rivero-Martin M. J. (20160922). [Phenotypic variability of the 1q21.1 microdeletion syndrome in members of the same family: relevance of detection of neuropsychiatric disorders for diagnosis of genetic syndromes]. : Revista de neurologia.

Chicago

Natera-De Benito Daniel, Vidal-Esteban Arantxa, Sanchez-Del Pozo Jaime, Moreno-Garcia Marta, Suela-Rubio Javier, Cruz-Rojo Jaime and Rivero-Martin María José. 20160922. [Phenotypic variability of the 1q21.1 microdeletion syndrome in members of the same family: relevance of detection of neuropsychiatric disorders for diagnosis of genetic syndromes]. : Revista de neurologia.

Harvard

Natera-De Benito D., Vidal-Esteban A., Sanchez-Del Pozo J., Moreno-Garcia M., Suela-Rubio J., Cruz-Rojo J. and Rivero-Martin M. J. (20160922). [Phenotypic variability of the 1q21.1 microdeletion syndrome in members of the same family: relevance of detection of neuropsychiatric disorders for diagnosis of genetic syndromes]. : Revista de neurologia.

MLA

Natera-De Benito Daniel, Vidal-Esteban Arantxa, Sanchez-Del Pozo Jaime, Moreno-Garcia Marta, Suela-Rubio Javier, Cruz-Rojo Jaime and Rivero-Martin María José. [Phenotypic variability of the 1q21.1 microdeletion syndrome in members of the same family: relevance of detection of neuropsychiatric disorders for diagnosis of genetic syndromes]. : Revista de neurologia. 20160922.