Cita APA

Dalamon, V. K., Buonfiglio, P., Larralde, M., Craig, P. O., Lotersztein, V., Choate, K., . . . Elgoyhen, A. B. (2016). Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: A case report. Web

Citación estilo Chicago

Dalamon, Viviana Karina, Paula Buonfiglio, Margarita Larralde, Patricio Oliver Craig, Vanesa Lotersztein, Keith Choate, Norma Pallares, Vicente Diamante, and Ana Belen Elgoyhen. Connexin 26 (GJB2) Mutation in an Argentinean Patient With Keratitis-ichthyosis-deafness (KID) Syndrome: A Case Report. 2016.

Cita MLA

Dalamon, Viviana Karina, et al. Connexin 26 (GJB2) Mutation in an Argentinean Patient With Keratitis-ichthyosis-deafness (KID) Syndrome: A Case Report. 2016.