Cita APA

Borges, M. d. F., Domene, H. M., Scaglia, P. A., Lara, B. H. J., Palhares, H. M. d. C., Aguiar, A. S. V., . . . Marqui, A. B. T. d. (2019). A recurrent mutation in TSHB gene underlying central congenital hypoyhyroidism undetectable in neonatal screening. Web

Citación estilo Chicago

Borges, Maria de Fátima, Horacio Mario Domene, Paula Alejandra Scaglia, Beatriz Hallal Jorge Lara, Heloísa Marcelina da Cunha Palhares, Andréia Santos Vasconcelos Aguiar, Amanda Gonçalves Lacerda Ferreira, Marília Matos Oliveira, and Alessandra Bernadete Trovó de Marqui. A Recurrent Mutation in TSHB Gene Underlying Central Congenital Hypoyhyroidism Undetectable in Neonatal Screening. 2019.

Cita MLA

Borges, Maria de Fátima, et al. A Recurrent Mutation in TSHB Gene Underlying Central Congenital Hypoyhyroidism Undetectable in Neonatal Screening. 2019.