Source: Abstracts. Conference titles: European Human Genetics Conference. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, MALFORMAÇÕES, DOENÇAS GENÉTICAS
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TAVARES, Vanessa Luiza et al. Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. 2014, Anais.. Milan: ESHG, 2014. . Acesso em: 02 nov. 2024.APA
Tavares, V. L., Gordon, C. T., Torres, T., Voisin, N., Bertola, D., Ceide, R. M. Z., et al. (2014). Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. In Abstracts. Milan: ESHG.NLM
Tavares VL, Gordon CT, Torres T, Voisin N, Bertola D, Ceide RMZ, Tan TY, Heggie AAC, Propst E, Papsin BC, Nakata NMK, Guion-Almeida ML, Pittoli SVP, Lyonnet S, Amiel J, Passos-Bueno MR. Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. Abstracts. 2014 ;[citado 2024 nov. 02 ]Vancouver
Tavares VL, Gordon CT, Torres T, Voisin N, Bertola D, Ceide RMZ, Tan TY, Heggie AAC, Propst E, Papsin BC, Nakata NMK, Guion-Almeida ML, Pittoli SVP, Lyonnet S, Amiel J, Passos-Bueno MR. Novel mutations in GNAI3 in patients with Auriculocondylar Syndrome suggest a dominant negative effect with disruption of GTP/GDP binding. Abstracts. 2014 ;[citado 2024 nov. 02 ]