Dalamón, V. K., Buonfiglio, P., Larralde, M., Craig, P., 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. BMC Med Genet.
Citação norma ChicagoDalamón, Viviana Karina, Paula Buonfiglio, Margarita Larralde, Patricio Craig, Vanesa Lotersztein, Keith Choate, Norma Pallares, Vicente Diamante, and Ana Belén Elgoyhen. "Connexin 26 (GJB2) Mutation in an Argentinean Patient With Keratitis-ichthyosis-deafness (KID) Syndrome: A Case Report." BMC Med Genet 2016.
Citação norma MLADalamón, Viviana Karina, et al. "Connexin 26 (GJB2) Mutation in an Argentinean Patient With Keratitis-ichthyosis-deafness (KID) Syndrome: A Case Report." BMC Med Genet 2016.