Cita APA

Gil Rodríguez, M. C., Deardorff, M. A., Ansari, M., Tan, C. A., Parenti, I., Baquero Montoya, C., . . . Pié, J. (2015). De novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia De Lange Syndrome-Overlapping Phenotypes. Web

Citación estilo Chicago

Gil Rodríguez, María Concepción, et al. De Novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia De Lange Syndrome-Overlapping Phenotypes. 2015.

Cita MLA

Gil Rodríguez, María Concepción, et al. De Novo Heterozygous Mutations in SMC3 Cause a Range of Cornelia De Lange Syndrome-Overlapping Phenotypes. 2015.