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Artigo de periodico
Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome (2011)
Teixeira, L. V. S.; Mandelbaum, K. L.; Pereira, Lygia da Veiga ; Perez, A B A
Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TEIXEIRA, L. V. S. et al. Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome. Brazilian Journal of Medical and Biological Research, v. 44, n. 8, p. 793-800, 2011Tradução . . Disponível em: https://doi.org/10.1590/S0100-879X2011007500095. Acesso em: 25 out. 2025.
APA
Teixeira, L. V. S., Mandelbaum, K. L., Pereira, L. da V., & Perez, A. B. A. (2011). Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome. Brazilian Journal of Medical and Biological Research, 44( 8), 793-800. doi:10.1590/S0100-879X2011007500095
NLM
Teixeira LVS, Mandelbaum KL, Pereira L da V, Perez ABA. Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 8): 793-800.[citado 2025 out. 25 ] Available from: https://doi.org/10.1590/S0100-879X2011007500095
Vancouver
Teixeira LVS, Mandelbaum KL, Pereira L da V, Perez ABA. Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome [Internet]. Brazilian Journal of Medical and Biological Research. 2011 ; 44( 8): 793-800.[citado 2025 out. 25 ] Available from: https://doi.org/10.1590/S0100-879X2011007500095
Trabalho de evento-resumo periodico
Detection of 5 mutations on fbn-1 gene in Marfan syndrome patients (1996)
Perez, A B A; Pereira, Lygia da Veiga ; Passos-Bueno, Maria Rita ; Brunoni, D; Zatz, Mayana
Source: Brazilian Journal of Genetics = Revista Brasileira de Genética. Conference titles: International Congress of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREZ, A B A et al. Detection of 5 mutations on fbn-1 gene in Marfan syndrome patients. Brazilian Journal of Genetics = Revista Brasileira de Genética. [S.l.]: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 25 out. 2025. , 1996
APA
Perez, A. B. A., Pereira, L. da V., Passos-Bueno, M. R., Brunoni, D., & Zatz, M. (1996). Detection of 5 mutations on fbn-1 gene in Marfan syndrome patients. Brazilian Journal of Genetics = Revista Brasileira de Genética. Instituto de Biociências, Universidade de São Paulo.
NLM
Perez ABA, Pereira L da V, Passos-Bueno MR, Brunoni D, Zatz M. Detection of 5 mutations on fbn-1 gene in Marfan syndrome patients. Brazilian Journal of Genetics = Revista Brasileira de Genética. 1996 ; 19( 2 suppl.): 246.[citado 2025 out. 25 ]
Vancouver
Perez ABA, Pereira L da V, Passos-Bueno MR, Brunoni D, Zatz M. Detection of 5 mutations on fbn-1 gene in Marfan syndrome patients. Brazilian Journal of Genetics = Revista Brasileira de Genética. 1996 ; 19( 2 suppl.): 246.[citado 2025 out. 25 ]
Artigo de periodico
Limg deficiency with or without mobius sequence in seven brazilian children associated with misoprostol use in the first trimester of pregnancy (1993)
Gonzalez, Claudette Hajaj; Vargas, F R; Perez, A B A; Kim, C A; Brunoni, D; Dias, M. J. M; Leone, C R; Correa Neto, J; Llerena Junior, J C; Almeida, J C C
Source: American Journal of Medical Genetics. Unidade: FM
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GONZALEZ, Claudette Hajaj et al. Limg deficiency with or without mobius sequence in seven brazilian children associated with misoprostol use in the first trimester of pregnancy. American Journal of Medical Genetics, v. 47, n. 1 , p. 59-64, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320470113. Acesso em: 25 out. 2025.
APA
Gonzalez, C. H., Vargas, F. R., Perez, A. B. A., Kim, C. A., Brunoni, D., Dias, M. J. M., et al. (1993). Limg deficiency with or without mobius sequence in seven brazilian children associated with misoprostol use in the first trimester of pregnancy. American Journal of Medical Genetics, 47( 1 ), 59-64. doi:10.1002/ajmg.1320470113
NLM
Gonzalez CH, Vargas FR, Perez ABA, Kim CA, Brunoni D, Dias MJM, Leone CR, Correa Neto J, Llerena Junior JC, Almeida JCC. Limg deficiency with or without mobius sequence in seven brazilian children associated with misoprostol use in the first trimester of pregnancy [Internet]. American Journal of Medical Genetics. 1993 ;47( 1 ): 59-64.[citado 2025 out. 25 ] Available from: https://doi.org/10.1002/ajmg.1320470113
Vancouver
Gonzalez CH, Vargas FR, Perez ABA, Kim CA, Brunoni D, Dias MJM, Leone CR, Correa Neto J, Llerena Junior JC, Almeida JCC. Limg deficiency with or without mobius sequence in seven brazilian children associated with misoprostol use in the first trimester of pregnancy [Internet]. American Journal of Medical Genetics. 1993 ;47( 1 ): 59-64.[citado 2025 out. 25 ] Available from: https://doi.org/10.1002/ajmg.1320470113

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