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Artigo de periodico
Detection of germline variants in Brazilian breast cancer patients using multigene panel testing (2022)
Guindalini, Rodrigo Santa Cruz; Viana, Danilo Vilela; Kitajima, Joao Paulo Fumio Whitaker; Rocha, Vinicius Marques; Lopez, Rossana Veronica Mendoza; Zheng, Yonglan; Freitas, Erika; Monteiro, Fabiola Paoli Mendes; Valim, Andre; Folgueira, Maria Aparecida Azevedo Koike
Source: Scientific reports. Unidade: FM
Subjects: GENES, NEOPLASIAS MAMÁRIAS, PREDISPOSIÇÃO GENÉTICA PARA DOENÇA, GAMETAS, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUINDALINI, Rodrigo Santa Cruz et al. Detection of germline variants in Brazilian breast cancer patients using multigene panel testing. Scientific reports, v. 12, n. 1, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41598-022-07383-1. Acesso em: 10 nov. 2024.
APA
Guindalini, R. S. C., Viana, D. V., Kitajima, J. P. F. W., Rocha, V. M., Lopez, R. V. M., Zheng, Y., et al. (2022). Detection of germline variants in Brazilian breast cancer patients using multigene panel testing. Scientific reports, 12( 1). doi:10.1038/s41598-022-07383-1
NLM
Guindalini RSC, Viana DV, Kitajima JPFW, Rocha VM, Lopez RVM, Zheng Y, Freitas E, Monteiro FPM, Valim A, Folgueira MAAK. Detection of germline variants in Brazilian breast cancer patients using multigene panel testing [Internet]. Scientific reports. 2022 ; 12( 1):[citado 2024 nov. 10 ] Available from: https://doi.org/10.1038/s41598-022-07383-1
Vancouver
Guindalini RSC, Viana DV, Kitajima JPFW, Rocha VM, Lopez RVM, Zheng Y, Freitas E, Monteiro FPM, Valim A, Folgueira MAAK. Detection of germline variants in Brazilian breast cancer patients using multigene panel testing [Internet]. Scientific reports. 2022 ; 12( 1):[citado 2024 nov. 10 ] Available from: https://doi.org/10.1038/s41598-022-07383-1
Artigo de periodico
Genomic monitoring unveil the early detection of the SARS-CoV-2 B.1.351 (beta) variant (20H/501Y.V2) in Brazil (2021)
Slavov, Svetoslav Nanev ; Patané, José Salvatore Leister; Bezerra, Rafael dos Santos; Giovanetti, Marta; Fonseca, Vagner; Martins, Antonio Jorge; Viala, Vincent Louis ; Rodrigues, Evandra Strazza ; Santos, Elaine Vieira ; Barros, Cláudia Renata dos Santos ; Marqueze, Elaine Cristina ; Santos, Bibiana; Aburjaile, Flávia Figueira; Neto, Raul M.; Moretti, Débora Botequio ; Haddad, Ricardo; Calado, Rodrigo Tocantins ; Kitajima, João Paulo; Freitas, Erika; Schlesinger, David; Alcantara, Luiz Carlos Junior; Elias, Maria Carolina ; Sampaio, Sandra Coccuzzo; Kashima, Simone ; Covas, Dimas Tadeu
Source: Journal of Medical Virology. Unidades: FMRP, BIOTECNOLOGIA
Subjects: COVID-19, GENÔMICA, SEQUENCIAMENTO GENÉTICO, PANDEMIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SLAVOV, Svetoslav Nanev et al. Genomic monitoring unveil the early detection of the SARS-CoV-2 B.1.351 (beta) variant (20H/501Y.V2) in Brazil. Journal of Medical Virology, v. 93, n. 12, p. 6782-6787, 2021Tradução . . Disponível em: https://doi.org/10.1002/jmv.27190. Acesso em: 10 nov. 2024.
APA
Slavov, S. N., Patané, J. S. L., Bezerra, R. dos S., Giovanetti, M., Fonseca, V., Martins, A. J., et al. (2021). Genomic monitoring unveil the early detection of the SARS-CoV-2 B.1.351 (beta) variant (20H/501Y.V2) in Brazil. Journal of Medical Virology, 93( 12), 6782-6787. doi:10.1002/jmv.27190
NLM
Slavov SN, Patané JSL, Bezerra R dos S, Giovanetti M, Fonseca V, Martins AJ, Viala VL, Rodrigues ES, Santos EV, Barros CR dos S, Marqueze EC, Santos B, Aburjaile FF, Neto RM, Moretti DB, Haddad R, Calado RT, Kitajima JP, Freitas E, Schlesinger D, Alcantara LCJ, Elias MC, Sampaio SC, Kashima S, Covas DT. Genomic monitoring unveil the early detection of the SARS-CoV-2 B.1.351 (beta) variant (20H/501Y.V2) in Brazil [Internet]. Journal of Medical Virology. 2021 ; 93( 12): 6782-6787.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1002/jmv.27190
Vancouver
Slavov SN, Patané JSL, Bezerra R dos S, Giovanetti M, Fonseca V, Martins AJ, Viala VL, Rodrigues ES, Santos EV, Barros CR dos S, Marqueze EC, Santos B, Aburjaile FF, Neto RM, Moretti DB, Haddad R, Calado RT, Kitajima JP, Freitas E, Schlesinger D, Alcantara LCJ, Elias MC, Sampaio SC, Kashima S, Covas DT. Genomic monitoring unveil the early detection of the SARS-CoV-2 B.1.351 (beta) variant (20H/501Y.V2) in Brazil [Internet]. Journal of Medical Virology. 2021 ; 93( 12): 6782-6787.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1002/jmv.27190
Artigo de periodico
Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations (2020)
Monteiro, Fabiola P; Curry, Cynthia J; Hevner, Robert; Elliott, Stephen; Fisher, Jamie H; Turocy, John; Dobyns, William B; Costa, Larissa A; Freitas, Erika; Kitajima, Joao Paulo; Kok, Fernando
Source: European journal of medical genetics. Unidade: FM
Subjects: ANORMALIDADES DO SISTEMA NERVOSO, ANORMALIDADES MUSCULOSQUELÉTICAS, ADENOSINA TRIFOSFATO, ERITROBLASTOSE FETAL, MICROCEFALIA, CÓRTEX CEREBRAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MONTEIRO, Fabiola P et al. Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. European journal of medical genetics, v. 63, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2019.01.014. Acesso em: 10 nov. 2024.
APA
Monteiro, F. P., Curry, C. J., Hevner, R., Elliott, S., Fisher, J. H., Turocy, J., et al. (2020). Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. European journal of medical genetics, 63( 1). doi:10.1016/j.ejmg.2019.01.014
NLM
Monteiro FP, Curry CJ, Hevner R, Elliott S, Fisher JH, Turocy J, Dobyns WB, Costa LA, Freitas E, Kitajima JP, Kok F. Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations [Internet]. European journal of medical genetics. 2020 ; 63( 1):[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmg.2019.01.014
Vancouver
Monteiro FP, Curry CJ, Hevner R, Elliott S, Fisher JH, Turocy J, Dobyns WB, Costa LA, Freitas E, Kitajima JP, Kok F. Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations [Internet]. European journal of medical genetics. 2020 ; 63( 1):[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejmg.2019.01.014

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