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LUCHS, Adriana e SABINO, Ester Cerdeira. Wuhan large pig roundworm virus identified in human feces in Brazil. Virus genes, v. 54, n. 3, p. 470-473, 2018Tradução . . Disponível em: https://doi.org/10.1007/s11262-018-1557-0. Acesso em: 19 out. 2024.
APA
Luchs, A., & Sabino, E. C. (2018). Wuhan large pig roundworm virus identified in human feces in Brazil. Virus genes, 54( 3), 470-473. doi:10.1007/s11262-018-1557-0
NLM
Luchs A, Sabino EC. Wuhan large pig roundworm virus identified in human feces in Brazil [Internet]. Virus genes. 2018 ; 54( 3): 470-473.[citado 2024 out. 19 ] Available from: https://doi.org/10.1007/s11262-018-1557-0
Vancouver
Luchs A, Sabino EC. Wuhan large pig roundworm virus identified in human feces in Brazil [Internet]. Virus genes. 2018 ; 54( 3): 470-473.[citado 2024 out. 19 ] Available from: https://doi.org/10.1007/s11262-018-1557-0
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ESTEPHAN, Eduardo de Paula et al. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome. Journal of neurology, v. 265, n. 3, p. 708-713, 2018Tradução . . Disponível em: https://doi.org/10.1007/s00415-018-8736-8. Acesso em: 19 out. 2024.
APA
Estephan, E. de P., Marchiori, P. E., Reed, U. C., & Zanoteli, E. (2018). A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome. Journal of neurology, 265( 3), 708-713. doi:10.1007/s00415-018-8736-8
NLM
Estephan E de P, Marchiori PE, Reed UC, Zanoteli E. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome [Internet]. Journal of neurology. 2018 ; 265( 3): 708-713.[citado 2024 out. 19 ] Available from: https://doi.org/10.1007/s00415-018-8736-8
Vancouver
Estephan E de P, Marchiori PE, Reed UC, Zanoteli E. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome [Internet]. Journal of neurology. 2018 ; 265( 3): 708-713.[citado 2024 out. 19 ] Available from: https://doi.org/10.1007/s00415-018-8736-8
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ALBUQUERQUE, Ingrid de Campos et al. Mutation in the S gene a determinant of the hepatitis B virus associated with concomitant HBsAg and anti-HBs in a population in Northeastern Brazil. Journal of Medical Virology, v. 89, n. 3, p. 458-462, 2017Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/jmv.24653/epdf. Acesso em: 19 out. 2024.
APA
Albuquerque, I. de C., Sousa, M. T., Santos, M. D. C., Nunes, J. D. C., Moraes, M. J. D., Gomes-Gouvêa, M. S., et al. (2017). Mutation in the S gene a determinant of the hepatitis B virus associated with concomitant HBsAg and anti-HBs in a population in Northeastern Brazil. Journal of Medical Virology, 89( 3), 458-462. doi:10.1002/jmv.24653
NLM
Albuquerque I de C, Sousa MT, Santos MDC, Nunes JDC, Moraes MJD, Gomes-Gouvêa MS, Pinho JRR, Carrilho FJ, Fonseca LMB, Ferreira A de SP. Mutation in the S gene a determinant of the hepatitis B virus associated with concomitant HBsAg and anti-HBs in a population in Northeastern Brazil [Internet]. Journal of Medical Virology. 2017 ; 89( 3): 458-462.[citado 2024 out. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/jmv.24653/epdf
Vancouver
Albuquerque I de C, Sousa MT, Santos MDC, Nunes JDC, Moraes MJD, Gomes-Gouvêa MS, Pinho JRR, Carrilho FJ, Fonseca LMB, Ferreira A de SP. Mutation in the S gene a determinant of the hepatitis B virus associated with concomitant HBsAg and anti-HBs in a population in Northeastern Brazil [Internet]. Journal of Medical Virology. 2017 ; 89( 3): 458-462.[citado 2024 out. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/jmv.24653/epdf
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SOARES, Diogo C. et al. Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome. Journal of Inherited Metabolic Disease, v. 40, n. , p. 461-462, 2017Tradução . . Disponível em: https://doi.org/10.1007%2Fs10545-016-9996-z. Acesso em: 19 out. 2024.
APA
Soares, D. C., Stroparo, M. N., Lian, Y. C., Takakura, C. Y., Wolf, S., Betz, R., & Kim, C. A. (2017). Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome. Journal of Inherited Metabolic Disease, 40( ), 461-462. doi:10.1007%2Fs10545-016-9996-z
NLM
Soares DC, Stroparo MN, Lian YC, Takakura CY, Wolf S, Betz R, Kim CA. Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome [Internet]. Journal of Inherited Metabolic Disease. 2017 ; 40( ): 461-462.[citado 2024 out. 19 ] Available from: https://doi.org/10.1007%2Fs10545-016-9996-z
Vancouver
Soares DC, Stroparo MN, Lian YC, Takakura CY, Wolf S, Betz R, Kim CA. Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome [Internet]. Journal of Inherited Metabolic Disease. 2017 ; 40( ): 461-462.[citado 2024 out. 19 ] Available from: https://doi.org/10.1007%2Fs10545-016-9996-z
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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NUNES, Luisa Mesquita et al. A new insight on CFTR allele frequency in Brazil through next generation sequencing. Pediatric pulmonology. New York: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/ppul.23409/epdf. Acesso em: 19 out. 2024. , 2016
APA
Nunes, L. M., Ribeiro, R., Sabino, E., Niewiandonski, V. D. T., Yamamoto, G. L., & Silva Filho, L. V. R. F. da. (2016). A new insight on CFTR allele frequency in Brazil through next generation sequencing. Pediatric pulmonology. New York: Faculdade de Medicina, Universidade de São Paulo. doi:10.1002/ppul.23409
NLM
Nunes LM, Ribeiro R, Sabino E, Niewiandonski VDT, Yamamoto GL, Silva Filho LVRF da. A new insight on CFTR allele frequency in Brazil through next generation sequencing [Internet]. Pediatric pulmonology. 2016 ; 51( suppl. 42): S18.[citado 2024 out. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ppul.23409/epdf
Vancouver
Nunes LM, Ribeiro R, Sabino E, Niewiandonski VDT, Yamamoto GL, Silva Filho LVRF da. A new insight on CFTR allele frequency in Brazil through next generation sequencing [Internet]. Pediatric pulmonology. 2016 ; 51( suppl. 42): S18.[citado 2024 out. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/ppul.23409/epdf
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MORAES-VASCONCELOS, Dewton et al. MCM4 deficiency: a rare variant of immunodeficiency of NK cells associated to proportionate nanism and adrenal insufficiency. description of the first case in Brazil. Journal of Clinical Immunology. New York: Springer. Disponível em: https://doi.org/10.1007/s10875-016-0237-x. Acesso em: 19 out. 2024. , 2016
APA
Moraes-Vasconcelos, D., Ribeiro, R., Rigato, P. O., Pinichi, P., Aoki, V., Takaoka, R., et al. (2016). MCM4 deficiency: a rare variant of immunodeficiency of NK cells associated to proportionate nanism and adrenal insufficiency. description of the first case in Brazil. Journal of Clinical Immunology. New York: Springer. doi:10.1007/s10875-016-0237-x
NLM
Moraes-Vasconcelos D, Ribeiro R, Rigato PO, Pinichi P, Aoki V, Takaoka R, Duarte AJ da S, Sabino EC. MCM4 deficiency: a rare variant of immunodeficiency of NK cells associated to proportionate nanism and adrenal insufficiency. description of the first case in Brazil [Internet]. Journal of Clinical Immunology. 2016 ; 36( 3): 324.[citado 2024 out. 19 ] Available from: https://doi.org/10.1007/s10875-016-0237-x
Vancouver
Moraes-Vasconcelos D, Ribeiro R, Rigato PO, Pinichi P, Aoki V, Takaoka R, Duarte AJ da S, Sabino EC. MCM4 deficiency: a rare variant of immunodeficiency of NK cells associated to proportionate nanism and adrenal insufficiency. description of the first case in Brazil [Internet]. Journal of Clinical Immunology. 2016 ; 36( 3): 324.[citado 2024 out. 19 ] Available from: https://doi.org/10.1007/s10875-016-0237-x
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LIPHAUS, Bernadete L. et al. Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus. Clinics, v. 70, n. 3, p. 220-227, 2015Tradução . . Disponível em: https://doi.org/10.6061/clinics/2015(03)12. Acesso em: 19 out. 2024.
APA
Liphaus, B. L., Umetsu, N., Jesus, A. A., Bando, S. Y., Silva, C. A., & Carneiro-Sampaio, M. (2015). Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus. Clinics, 70( 3), 220-227. doi:10.6061/clinics/2015(03)12
NLM
Liphaus BL, Umetsu N, Jesus AA, Bando SY, Silva CA, Carneiro-Sampaio M. Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus [Internet]. Clinics. 2015 ; 70( 3): 220-227.[citado 2024 out. 19 ] Available from: https://doi.org/10.6061/clinics/2015(03)12
Vancouver
Liphaus BL, Umetsu N, Jesus AA, Bando SY, Silva CA, Carneiro-Sampaio M. Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus [Internet]. Clinics. 2015 ; 70( 3): 220-227.[citado 2024 out. 19 ] Available from: https://doi.org/10.6061/clinics/2015(03)12
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GUINDALINI, Rodrigo Santa Cruz et al. Frequency of CDH1 germline mutations in diffuse gastric cancer in Brazil. Journal of Clinical Oncology. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://meeting.ascopubs.org/cgi/content/abstract/33/15_suppl/e12535?sid=b24c1c59-00ab-4768-be20-3775ba7e8838. Acesso em: 19 out. 2024. , 2015
APA
Guindalini, R. S. C., Pasini, F. S., De Gouvea, A. C. R. C., Branas, P. A., Cormedi, M. C. V., Maistro, S., et al. (2015). Frequency of CDH1 germline mutations in diffuse gastric cancer in Brazil. Journal of Clinical Oncology. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://meeting.ascopubs.org/cgi/content/abstract/33/15_suppl/e12535?sid=b24c1c59-00ab-4768-be20-3775ba7e8838
NLM
Guindalini RSC, Pasini FS, De Gouvea ACRC, Branas PA, Cormedi MCV, Maistro S, Katayama MLH, Encinas G, Nagy T, Estevez-Diz MDP, Safatle-Ribeiro AV, Ribeiro U, Folgueira MAAK. Frequency of CDH1 germline mutations in diffuse gastric cancer in Brazil [Internet]. Journal of Clinical Oncology. 2015 ; 33( 15S ):[citado 2024 out. 19 ] Available from: http://meeting.ascopubs.org/cgi/content/abstract/33/15_suppl/e12535?sid=b24c1c59-00ab-4768-be20-3775ba7e8838
Vancouver
Guindalini RSC, Pasini FS, De Gouvea ACRC, Branas PA, Cormedi MCV, Maistro S, Katayama MLH, Encinas G, Nagy T, Estevez-Diz MDP, Safatle-Ribeiro AV, Ribeiro U, Folgueira MAAK. Frequency of CDH1 germline mutations in diffuse gastric cancer in Brazil [Internet]. Journal of Clinical Oncology. 2015 ; 33( 15S ):[citado 2024 out. 19 ] Available from: http://meeting.ascopubs.org/cgi/content/abstract/33/15_suppl/e12535?sid=b24c1c59-00ab-4768-be20-3775ba7e8838
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MANGONE, Flavia Rotea et al. ATM gene mutations in sporadic breast cancer patients from Brazil. Springer Plus, v. 4, 2015Tradução . . Disponível em: https://doi.org/10.1186/s40064-015-0787-z. Acesso em: 19 out. 2024.
APA
Mangone, F. R., Miracca, E. C., Feilotter, H. E., Mulligan, L. M., & Nagai, M. A. (2015). ATM gene mutations in sporadic breast cancer patients from Brazil. Springer Plus, 4. doi:10.1186/s40064-015-0787-z
NLM
Mangone FR, Miracca EC, Feilotter HE, Mulligan LM, Nagai MA. ATM gene mutations in sporadic breast cancer patients from Brazil [Internet]. Springer Plus. 2015 ; 4[citado 2024 out. 19 ] Available from: https://doi.org/10.1186/s40064-015-0787-z
Vancouver
Mangone FR, Miracca EC, Feilotter HE, Mulligan LM, Nagai MA. ATM gene mutations in sporadic breast cancer patients from Brazil [Internet]. Springer Plus. 2015 ; 4[citado 2024 out. 19 ] Available from: https://doi.org/10.1186/s40064-015-0787-z
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GONZAGA, Ana Denise Gomes et al. Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria. Annals of Human Genetics, v. 79, n. 3, p. 162-172, 2015Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/ahg.12102/epdf. Acesso em: 19 out. 2024.
APA
Gonzaga, A. D. G., Amorim, L. M. da F. de, Fonseca, A. B. M., Nogueira, T. L. S., Pereira, O. M. D., Nagai, M. A., et al. (2015). Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria. Annals of Human Genetics, 79( 3), 162-172. doi:10.1111/ahg.12102
NLM
Gonzaga ADG, Amorim LM da F de, Fonseca ABM, Nogueira TLS, Pereira OMD, Nagai MA, Barretto OC de O, Ribeiro GS. Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria [Internet]. Annals of Human Genetics. 2015 ; 79( 3): 162-172.[citado 2024 out. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/ahg.12102/epdf
Vancouver
Gonzaga ADG, Amorim LM da F de, Fonseca ABM, Nogueira TLS, Pereira OMD, Nagai MA, Barretto OC de O, Ribeiro GS. Hydroxymethylbilane Synthase Gene Mutations and Polymorphisms in Brazilian Families with Acute Intermittent Porphyria [Internet]. Annals of Human Genetics. 2015 ; 79( 3): 162-172.[citado 2024 out. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/ahg.12102/epdf
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LIMA-STEIN, Mariana Leão de et al. In Vivo HIV-1 Hypermutation and Viral Loads Among Antiretroviral-Naive Brazilian Patients. AIDS RESEARCH AND HUMAN RETROVIRUSES, v. 30, n. 9, p. 867-880, 2014Tradução . . Disponível em: http://online.liebertpub.com/doi/pdfplus/10.1089/aid.2013.0241. Acesso em: 19 out. 2024.
APA
Lima-Stein, M. L. de, Alkmim, W. T., Bizinoto, M. C. de S., Lopez, L. F., Burattini, M. N., Maricato, J. T., et al. (2014). In Vivo HIV-1 Hypermutation and Viral Loads Among Antiretroviral-Naive Brazilian Patients. AIDS RESEARCH AND HUMAN RETROVIRUSES, 30( 9), 867-880. doi:10.1089/aid.2013.0241
NLM
Lima-Stein ML de, Alkmim WT, Bizinoto MC de S, Lopez LF, Burattini MN, Maricato JT, Giron L, Sucupira MCA, Diaz RS, Janini LM. In Vivo HIV-1 Hypermutation and Viral Loads Among Antiretroviral-Naive Brazilian Patients [Internet]. AIDS RESEARCH AND HUMAN RETROVIRUSES. 2014 ; 30( 9): 867-880.[citado 2024 out. 19 ] Available from: http://online.liebertpub.com/doi/pdfplus/10.1089/aid.2013.0241
Vancouver
Lima-Stein ML de, Alkmim WT, Bizinoto MC de S, Lopez LF, Burattini MN, Maricato JT, Giron L, Sucupira MCA, Diaz RS, Janini LM. In Vivo HIV-1 Hypermutation and Viral Loads Among Antiretroviral-Naive Brazilian Patients [Internet]. AIDS RESEARCH AND HUMAN RETROVIRUSES. 2014 ; 30( 9): 867-880.[citado 2024 out. 19 ] Available from: http://online.liebertpub.com/doi/pdfplus/10.1089/aid.2013.0241
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SMID, J. et al. Phenotypic heterogeneity in a Brazilian family with a mutation in codon 102 of the prion protein gene. Brain Pathology. Zurich: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12183/pdf. Acesso em: 19 out. 2024. , 2014
APA
Smid, J., Landemberger, M. C., Martins, V. R., Schultz, R. R., Rosemberg. S.,, Chimelli, L., & Nitrini, R. (2014). Phenotypic heterogeneity in a Brazilian family with a mutation in codon 102 of the prion protein gene. Brain Pathology. Zurich: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://onlinelibrary.wiley.com/doi/10.1111/bpa.12183/pdf
NLM
Smid J, Landemberger MC, Martins VR, Schultz RR, Rosemberg. S., Chimelli L, Nitrini R. Phenotypic heterogeneity in a Brazilian family with a mutation in codon 102 of the prion protein gene [Internet]. Brain Pathology. 2014 ; 24 16.[citado 2024 out. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12183/pdf
Vancouver
Smid J, Landemberger MC, Martins VR, Schultz RR, Rosemberg. S., Chimelli L, Nitrini R. Phenotypic heterogeneity in a Brazilian family with a mutation in codon 102 of the prion protein gene [Internet]. Brain Pathology. 2014 ; 24 16.[citado 2024 out. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12183/pdf
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LANDEMBERGER, M. C. et al. Human prion diseases in Brazil. Brain Pathology. Zurich: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12184/pdf. Acesso em: 19 out. 2024. , 2014
APA
Landemberger, M. C., Machado, C. F., Smid, J., Gomes, H. R., Chimelli, L., Rosemberg. S.,, et al. (2014). Human prion diseases in Brazil. Brain Pathology. Zurich: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://onlinelibrary.wiley.com/doi/10.1111/bpa.12184/pdf
NLM
Landemberger MC, Machado CF, Smid J, Gomes HR, Chimelli L, Rosemberg. S., Nitrini R, Martins VR. Human prion diseases in Brazil [Internet]. Brain Pathology. 2014 ; 24 81.[citado 2024 out. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12184/pdf
Vancouver
Landemberger MC, Machado CF, Smid J, Gomes HR, Chimelli L, Rosemberg. S., Nitrini R, Martins VR. Human prion diseases in Brazil [Internet]. Brain Pathology. 2014 ; 24 81.[citado 2024 out. 19 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/bpa.12184/pdf
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FRAGOSO, Maria Candida B. V. et al. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients. European Journal of Endocrinology, v. 166, n. 1, p. 61-67, 2012Tradução . . Disponível em: https://doi.org/10.1530/EJE-11-0964. Acesso em: 19 out. 2024.
APA
Fragoso, M. C. B. V., Almeida, M. Q., Mazzuco, T. L., Mariani, B. M. P., Brito, L. P., Gonçalves, T. C., et al. (2012). Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients. European Journal of Endocrinology, 166( 1), 61-67. doi:10.1530/EJE-11-0964
NLM
Fragoso MCBV, Almeida MQ, Mazzuco TL, Mariani BMP, Brito LP, Gonçalves TC, Alencar GA, Lima L de O, Faria AM, Bourdeau I, Lucon AM, Freire DS, Latronico AC, Mendonca BB, Lacroix A, Lerario AM. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients [Internet]. European Journal of Endocrinology. 2012 ; 166( 1): 61-67.[citado 2024 out. 19 ] Available from: https://doi.org/10.1530/EJE-11-0964
Vancouver
Fragoso MCBV, Almeida MQ, Mazzuco TL, Mariani BMP, Brito LP, Gonçalves TC, Alencar GA, Lima L de O, Faria AM, Bourdeau I, Lucon AM, Freire DS, Latronico AC, Mendonca BB, Lacroix A, Lerario AM. Combined expression of BUB1B, DLG7, and PINK1 as predictors of poor outcome in adrenocortical tumors: validation in a Brazilian cohort of adult and pediatric patients [Internet]. European Journal of Endocrinology. 2012 ; 166( 1): 61-67.[citado 2024 out. 19 ] Available from: https://doi.org/10.1530/EJE-11-0964
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BITTENCOURT, Paulo Lisboa et al. Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis. Clinics, v. 64, n. 9, p. 837-841, 2009Tradução . . Disponível em: https://doi.org/10.1590/s1807-59322009000900003. Acesso em: 19 out. 2024.
APA
Bittencourt, P. L., Marin, M. L. C., Couto, C. A., Cançado, E. L. R., Carrilho, F. J., & Goldberg, A. C. (2009). Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis. Clinics, 64( 9), 837-841. doi:10.1590/s1807-59322009000900003
NLM
Bittencourt PL, Marin MLC, Couto CA, Cançado ELR, Carrilho FJ, Goldberg AC. Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis [Internet]. Clinics. 2009 ; 64( 9): 837-841.[citado 2024 out. 19 ] Available from: https://doi.org/10.1590/s1807-59322009000900003
Vancouver
Bittencourt PL, Marin MLC, Couto CA, Cançado ELR, Carrilho FJ, Goldberg AC. Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis [Internet]. Clinics. 2009 ; 64( 9): 837-841.[citado 2024 out. 19 ] Available from: https://doi.org/10.1590/s1807-59322009000900003
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RASKIN, Salmo et al. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients. Journal of cystic fibrosis, v. 7, n. 1, p. 15-22, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jcf.2007.03.006. Acesso em: 19 out. 2024.
APA
Raskin, S., Ferrari, L. P., Reis, F. C., Abreu, F., Marostica, P., Rozov, T., et al. (2008). Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients. Journal of cystic fibrosis, 7( 1), 15-22. doi:10.1016/j.jcf.2007.03.006
NLM
Raskin S, Ferrari LP, Reis FC, Abreu F, Marostica P, Rozov T, Cardieri J, Ludwing N, Valentin L, Rosario Filho NA, Camargo Neto E, Lewis E, Giugliani R, Diniz EMA, Culpi L, Phillip III JA, Chakraborty R. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients [Internet]. Journal of cystic fibrosis. 2008 ; 7( 1): 15-22.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/j.jcf.2007.03.006
Vancouver
Raskin S, Ferrari LP, Reis FC, Abreu F, Marostica P, Rozov T, Cardieri J, Ludwing N, Valentin L, Rosario Filho NA, Camargo Neto E, Lewis E, Giugliani R, Diniz EMA, Culpi L, Phillip III JA, Chakraborty R. Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients [Internet]. Journal of cystic fibrosis. 2008 ; 7( 1): 15-22.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/j.jcf.2007.03.006
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DEGUTI, Marta Mitiko. Doença de Wilson: aspectos demográficos e fenotípicos relacionados ao genótipo ATP7B e estudo do haplótipo em portadores da mutação L708P. 2004. Tese (Doutorado) – Universidade de São Paulo, São Paulo, 2004. Disponível em: http://www.teses.usp.br/teses/disponiveis/5/5147/tde-02052006-093857/. Acesso em: 19 out. 2024.
APA
Deguti, M. M. (2004). Doença de Wilson: aspectos demográficos e fenotípicos relacionados ao genótipo ATP7B e estudo do haplótipo em portadores da mutação L708P (Tese (Doutorado). Universidade de São Paulo, São Paulo. Recuperado de http://www.teses.usp.br/teses/disponiveis/5/5147/tde-02052006-093857/
NLM
Deguti MM. Doença de Wilson: aspectos demográficos e fenotípicos relacionados ao genótipo ATP7B e estudo do haplótipo em portadores da mutação L708P [Internet]. 2004 ;[citado 2024 out. 19 ] Available from: http://www.teses.usp.br/teses/disponiveis/5/5147/tde-02052006-093857/
Vancouver
Deguti MM. Doença de Wilson: aspectos demográficos e fenotípicos relacionados ao genótipo ATP7B e estudo do haplótipo em portadores da mutação L708P [Internet]. 2004 ;[citado 2024 out. 19 ] Available from: http://www.teses.usp.br/teses/disponiveis/5/5147/tde-02052006-093857/
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUTNISKY, Viviana J. et al. Two distinct compound heterozygous constellation (R277X / IVS34-1G>C and R277X / R1511X) in the thyroglobulin gene in affected individuals of a Brazilian kindred with congenital goiter and defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism, v. 89, n. 2, p. 646-657, 2004Tradução . . Acesso em: 19 out. 2024.
APA
Gutnisky, V. J., Moya, C. M., Rivolta, C. M., Domené, S., Varela, V., Toniolo, J. V., et al. (2004). Two distinct compound heterozygous constellation (R277X / IVS34-1G>C and R277X / R1511X) in the thyroglobulin gene in affected individuals of a Brazilian kindred with congenital goiter and defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism, 89( 2), 646-657.
NLM
Gutnisky VJ, Moya CM, Rivolta CM, Domené S, Varela V, Toniolo JV, Medeiros-Neto G, Targovnik HM. Two distinct compound heterozygous constellation (R277X / IVS34-1G>C and R277X / R1511X) in the thyroglobulin gene in affected individuals of a Brazilian kindred with congenital goiter and defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism. 2004 ; 89( 2): 646-657.[citado 2024 out. 19 ]
Vancouver
Gutnisky VJ, Moya CM, Rivolta CM, Domené S, Varela V, Toniolo JV, Medeiros-Neto G, Targovnik HM. Two distinct compound heterozygous constellation (R277X / IVS34-1G>C and R277X / R1511X) in the thyroglobulin gene in affected individuals of a Brazilian kindred with congenital goiter and defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism. 2004 ; 89( 2): 646-657.[citado 2024 out. 19 ]