The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss (2011)
- Authors:
- USP affiliated authors: CARVALHO, MÁRIO HENRIQUE BURLACCHINI DE - FM ; ZUGAIB, MARCELO - FM ; SHINOHARA, ELVIRA MARIA GUERRA - FCF
- Unidades: FM; FCF
- Subjects: POLIMORFISMO; ABORTO ESPONTÂNEO
- Language: Inglês
- Imprenta:
- Source:
- Título: Brazilian Journal of Pharmaceutical Sciences
- ISSN: 1984-8250
- Volume/Número/Paginação/Ano: v. 47, suppl. 1, p. 40 res. FCF076, 2011
- Conference titles: Science and Pharmaceutical Technology Meeting of the Pharmaceutical Sciences Faculty of the University of São Paulo
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ABNT
CAVALCANTE, Silvana Henrique et al. The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 27 jan. 2026. , 2011 -
APA
Cavalcante, S. H., Lázaro, R. J., Boacnin, M. do R., Carvalho, M. H. B. de, Amorim Filho, A., Zugaib, M., & Guerra-Shinohara, E. M. (2011). The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Cavalcante SH, Lázaro RJ, Boacnin M do R, Carvalho MHB de, Amorim Filho A, Zugaib M, Guerra-Shinohara EM. The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47 40 res. FCF076.[citado 2026 jan. 27 ] -
Vancouver
Cavalcante SH, Lázaro RJ, Boacnin M do R, Carvalho MHB de, Amorim Filho A, Zugaib M, Guerra-Shinohara EM. The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss. Brazilian Journal of Pharmaceutical Sciences. 2011 ; 47 40 res. FCF076.[citado 2026 jan. 27 ] - Association betweem polymorfisms related to hemostasis and the occurence of recurrent miscarriages
- Association between the polymorphisms MTHFR C677T, MTR A2756G and MTRR A66G with recurrent miscarriages
- Frequencies of autoantibodies in women with recurrent pregnancy losses
- The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss
- Association between the polymorphisms MTHFR c. 677C>T and MTHFR c. 1298A>C and haplotypes with recurrent miscarriages
- Association between polymorphisms in the transcobalamin II gene (TC2 C. 776C> G and C. TC267C>G) and methylenetetrahydrofolate reductase gene (MTHFR 677C>T) and risk of having recurrent miscarriages
- Effect of genetic polimorphisms related with folate metabolism(MTHFR, MTHFD1, RFC1) and their association with recurrent miscarriages
- Association between polymorphisms in the transcobalamin II gene (TC2 C. 776C> G and C.TC2 67C>G) and methylenetetrahydrofolate reductase gene (MTHFR C. MTHFR 677C>T) and risk of having recurrent miscarriages
- Frequency of autoantibodies in women with recurrent miscarriage history
- Polymorphisms in thrombin-activatable fibrinolysis inhibitor and plasminogen activator inhibitor type 1 in women with primary recurrent pregnancy loss
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