Fonte: Clinics. Nome do evento: Symposium Autoimmunity in Primary Immunodeficiences. Unidades: FMRP, FCFRP
Assuntos: MOLÉCULA (ANÁLISE), MUTAÇÃO
ABNT
MESCHEDE, I. P. et al. Molecular diagnosis of Griscelli syndrome in Brazilian patients and characterization of cellular phenotypes. Clinics. São Paulo: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 11 set. 2024. , 2007APA
Meschede, I. P., Nader, G. P. F., Santos, T. O., Pranchevivius, M. C., Larson, R. E., Castro, F. A. de, et al. (2007). Molecular diagnosis of Griscelli syndrome in Brazilian patients and characterization of cellular phenotypes. Clinics. São Paulo: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.NLM
Meschede IP, Nader GPF, Santos TO, Pranchevivius MC, Larson RE, Castro FA de, Pessoa F, Kok F, Gurgel-Gianetti J, Bonfim CMS, Roxo Júnior P, Espreáfico EM. Molecular diagnosis of Griscelli syndrome in Brazilian patients and characterization of cellular phenotypes. Clinics. 2007 ; 62 S43.[citado 2024 set. 11 ]Vancouver
Meschede IP, Nader GPF, Santos TO, Pranchevivius MC, Larson RE, Castro FA de, Pessoa F, Kok F, Gurgel-Gianetti J, Bonfim CMS, Roxo Júnior P, Espreáfico EM. Molecular diagnosis of Griscelli syndrome in Brazilian patients and characterization of cellular phenotypes. Clinics. 2007 ; 62 S43.[citado 2024 set. 11 ]