Fonte: Resumos. Nome do evento: ENDO - The Endocrine Society's Annual Meeting. Unidade: FM
Assunto: ENDOCRINOLOGIA
ABNT
SOUZA, Silvia C. A. L. et al. Screening of PTPN11 mutations in brazilian patients with noonan syndrome:: identification of a novel mutation (N58D). 2003, Anais.. Philadelphia: Faculdade de Medicina, Universidade de São Paulo, 2003. . Acesso em: 01 out. 2024.APA
Souza, S. C. A. L., Jorge, A. A., Ferreira, L. V., Arnhold, I. J. P., & Mendonça, B. B. (2003). Screening of PTPN11 mutations in brazilian patients with noonan syndrome:: identification of a novel mutation (N58D). In Resumos. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.NLM
Souza SCAL, Jorge AA, Ferreira LV, Arnhold IJP, Mendonça BB. Screening of PTPN11 mutations in brazilian patients with noonan syndrome:: identification of a novel mutation (N58D). Resumos. 2003 ;[citado 2024 out. 01 ]Vancouver
Souza SCAL, Jorge AA, Ferreira LV, Arnhold IJP, Mendonça BB. Screening of PTPN11 mutations in brazilian patients with noonan syndrome:: identification of a novel mutation (N58D). Resumos. 2003 ;[citado 2024 out. 01 ]