Cita APA

Urreizti, R., Cueto Gonzalez, A. M., Franco Valls, H., Mort Farre, S., Roca Ayats, N., Ponomarenko, J., . . . Balcells Comas, S. (2017). A de novo nonsense mutation in MAGEL2 in a patient initially diagnosed as Opitz-C: Similarities between Schaaf-Yang and Opitz-C syndromes.

Citación estilo Chicago

Urreizti, Roser, et al. A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed As Opitz-C: Similarities between Schaaf-Yang and Opitz-C Syndromes. 2017.

Cita MLA

Urreizti, Roser, et al. A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed As Opitz-C: Similarities between Schaaf-Yang and Opitz-C Syndromes. 2017.