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Trabalho de evento-resumo periodico
Screening of SPINK1 mutations indicate further heterogeneity for chronic pancreatitis (2002)
Bernardino, A L; Guarita, C. B.; Mott, C B; Pedroso, M. R. A.; Machado, Marcel Cerqueira César; Laudanna, Antônio Atílio; Tani, C. M.; Almeida, F. L.; Zatz, Mayana
Source: American Journal of Human Genetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: IB, FM
Subjects: PANCREATOPATIAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDINO, A L et al. Screening of SPINK1 mutations indicate further heterogeneity for chronic pancreatitis. American Journal of Human Genetics. Baltimore: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2002
APA
Bernardino, A. L., Guarita, C. B., Mott, C. B., Pedroso, M. R. A., Machado, M. C. C., Laudanna, A. A., et al. (2002). Screening of SPINK1 mutations indicate further heterogeneity for chronic pancreatitis. American Journal of Human Genetics. Baltimore: Instituto de Biociências, Universidade de São Paulo.
NLM
Bernardino AL, Guarita CB, Mott CB, Pedroso MRA, Machado MCC, Laudanna AA, Tani CM, Almeida FL, Zatz M. Screening of SPINK1 mutations indicate further heterogeneity for chronic pancreatitis. American Journal of Human Genetics. 2002 ; 71( 4): 480 res.1817.[citado 2024 nov. 01 ]
Vancouver
Bernardino AL, Guarita CB, Mott CB, Pedroso MRA, Machado MCC, Laudanna AA, Tani CM, Almeida FL, Zatz M. Screening of SPINK1 mutations indicate further heterogeneity for chronic pancreatitis. American Journal of Human Genetics. 2002 ; 71( 4): 480 res.1817.[citado 2024 nov. 01 ]
Trabalho de evento-resumo periodico
The effect of letethonin deficiency in LGMD-2G and the expession in other forms of muscular dystrophies and congenital myopathies (2000)
Velnzof, M.; Moreira, E.S.; Passos-Bueno, Maria Rita ; Faulkner, G.; Zanotoli, E.; Gurgel-Glanneti, J.; Ribeiro, A. F.; Silva, H.C.A.; Tsanaclis, Ana Maria Crous; Zatz, Mayana
Source: American Journal of Human Genetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: FM, IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VELNZOF, M. et al. The effect of letethonin deficiency in LGMD-2G and the expession in other forms of muscular dystrophies and congenital myopathies. American Journal of Human Genetics. Chicago: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2000
APA
Velnzof, M., Moreira, E. S., Passos-Bueno, M. R., Faulkner, G., Zanotoli, E., Gurgel-Glanneti, J., et al. (2000). The effect of letethonin deficiency in LGMD-2G and the expession in other forms of muscular dystrophies and congenital myopathies. American Journal of Human Genetics. Chicago: Faculdade de Medicina, Universidade de São Paulo.
NLM
Velnzof M, Moreira ES, Passos-Bueno MR, Faulkner G, Zanotoli E, Gurgel-Glanneti J, Ribeiro AF, Silva HCA, Tsanaclis AMC, Zatz M. The effect of letethonin deficiency in LGMD-2G and the expession in other forms of muscular dystrophies and congenital myopathies. American Journal of Human Genetics. 2000 ; 67( 4): 10.[citado 2024 nov. 01 ]
Vancouver
Velnzof M, Moreira ES, Passos-Bueno MR, Faulkner G, Zanotoli E, Gurgel-Glanneti J, Ribeiro AF, Silva HCA, Tsanaclis AMC, Zatz M. The effect of letethonin deficiency in LGMD-2G and the expession in other forms of muscular dystrophies and congenital myopathies. American Journal of Human Genetics. 2000 ; 67( 4): 10.[citado 2024 nov. 01 ]
Trabalho de evento-resumo periodico
Screening of CFTR and PRSS1 mutations in patients with pancreatitis (2000)
Bernardino, A L; Guarita, D; Mott, C; Machado, Marcel Cerqueira César; Laudanna, Antônio Atílio; Tani, C M; Miranda, K F; Almeida, F L; Zatz, Mayana
Source: American Journal of Human Genetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: IB, FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDINO, A L et al. Screening of CFTR and PRSS1 mutations in patients with pancreatitis. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2000
APA
Bernardino, A. L., Guarita, D., Mott, C., Machado, M. C. C., Laudanna, A. A., Tani, C. M., et al. (2000). Screening of CFTR and PRSS1 mutations in patients with pancreatitis. American Journal of Human Genetics. Chicago: Instituto de Biociências, Universidade de São Paulo.
NLM
Bernardino AL, Guarita D, Mott C, Machado MCC, Laudanna AA, Tani CM, Miranda KF, Almeida FL, Zatz M. Screening of CFTR and PRSS1 mutations in patients with pancreatitis. American Journal of Human Genetics. 2000 ; 67( 4): 361 R2018.[citado 2024 nov. 01 ]
Vancouver
Bernardino AL, Guarita D, Mott C, Machado MCC, Laudanna AA, Tani CM, Miranda KF, Almeida FL, Zatz M. Screening of CFTR and PRSS1 mutations in patients with pancreatitis. American Journal of Human Genetics. 2000 ; 67( 4): 361 R2018.[citado 2024 nov. 01 ]

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