Cita APA

Martín Nalda, A., Cueto Gonzalez, A. M., Colobran Oriol, R., Plaja Rustein, A., Castells Sarret, N., Rivière, J., . . . Marin Soria, J. L. (2019). Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency: Two years’ experience in Catalonia (Spain).

Citación estilo Chicago

Martín Nalda, Andrea, et al. Identification of 22q11.2 Deletion Syndrome Via Newborn Screening for Severe Combined Immunodeficiency: Two Years’ Experience in Catalonia (Spain). 2019.

Cita MLA

Martín Nalda, Andrea, et al. Identification of 22q11.2 Deletion Syndrome Via Newborn Screening for Severe Combined Immunodeficiency: Two Years’ Experience in Catalonia (Spain). 2019.