Marino, R. M., Garrido, N. P., Costanzo, M., Guercio, G. V., Juanes, M. H., Rocco, C. A., . . . Saraco, N. I. (2015). Five new cases of 46, XX aromatase deficiency: Clinical follow-up from birth to puberty, a novel mutation, and a founder effect. Web
Citación estilo ChicagoMarino, Roxana Marcela, et al. Five New Cases of 46, XX Aromatase Deficiency: Clinical Follow-up From Birth to Puberty, a Novel Mutation, and a Founder Effect. 2015.
Cita MLAMarino, Roxana Marcela, et al. Five New Cases of 46, XX Aromatase Deficiency: Clinical Follow-up From Birth to Puberty, a Novel Mutation, and a Founder Effect. 2015.
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