ReP USP - Resultado da busca

Artigo de periodico
Maxillary myxomas associated with MEN1 syndrome (2014)
Lourenço, D. M.; Toledo, R. A.; Sekiya, T.; Moraes, M. B.; Santana, L. S.; Toledo, S. P. A.
Fonte: Wiener Klinische Wochenschrift. Nome do evento: International workshop on multiple endocrine neoplasia and other rare endocrine tumors. Unidade: FM
Assuntos: GENES, OSSOS FACIAIS, NEOPLASIAS DO TECIDO CONJUNTIVO, MANDÍBULA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOURENÇO, D. M. et al. Maxillary myxomas associated with MEN1 syndrome. Wiener Klinische Wochenschrift, v. 126, n. 3, p. S142-S143, 2014Tradução . . Disponível em: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5. Acesso em: 01 out. 2024.
APA
Lourenço, D. M., Toledo, R. A., Sekiya, T., Moraes, M. B., Santana, L. S., & Toledo, S. P. A. (2014). Maxillary myxomas associated with MEN1 syndrome. Wiener Klinische Wochenschrift, 126( 3), S142-S143. Recuperado de http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
NLM
Lourenço DM, Toledo RA, Sekiya T, Moraes MB, Santana LS, Toledo SPA. Maxillary myxomas associated with MEN1 syndrome [Internet]. Wiener Klinische Wochenschrift. 2014 ; 126( 3): S142-S143.[citado 2024 out. 01 ] Available from: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
Vancouver
Lourenço DM, Toledo RA, Sekiya T, Moraes MB, Santana LS, Toledo SPA. Maxillary myxomas associated with MEN1 syndrome [Internet]. Wiener Klinische Wochenschrift. 2014 ; 126( 3): S142-S143.[citado 2024 out. 01 ] Available from: http://download.springer.com/static/pdf/98/art%253A10.1007%252Fs00508-014-0578-5.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00508-014-0578-5&token2=exp=1441028215~acl=%2Fstatic%2Fpdf%2F98%2Fart%25253A10.1007%25252Fs00508-014-0578-5.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00508-014-0578-5*~hmac=73d6878165a21b41ce52406bd29e650b2d7f444eeccde0e5517495f2244945e5
Trabalho de evento-resumo
MEN 1 gene is not implicated in adrenal hyperplasia associated with multiple endocrine neoplasia type 1 (2006)
Costa, Marcia Helena S.; Pinto, Emilia M.; Billerbeck, Ana Elisa; Mendonça, Berenice Bilharinho de; Junior, Delmar Muniz; Toledo, S. P. A.; Fragoso, Maria Candida B. V.
Fonte: Resumos. Nome do evento: ENDO 06 - Annual Meeting the endocrine society's. Unidade: FM
Assuntos: HIPERPLASIAS, GENES, ENDOCRINOPATIAS, NEOPLASIAS, RESUMOS (CONGRESSOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, Marcia Helena S. et al. MEN 1 gene is not implicated in adrenal hyperplasia associated with multiple endocrine neoplasia type 1. 2006, Anais.. Boston: Faculdade de Medicina, Universidade de São Paulo, 2006. . Acesso em: 01 out. 2024.
APA
Costa, M. H. S., Pinto, E. M., Billerbeck, A. E., Mendonça, B. B. de, Junior, D. M., Toledo, S. P. A., & Fragoso, M. C. B. V. (2006). MEN 1 gene is not implicated in adrenal hyperplasia associated with multiple endocrine neoplasia type 1. In Resumos. Boston: Faculdade de Medicina, Universidade de São Paulo.
NLM
Costa MHS, Pinto EM, Billerbeck AE, Mendonça BB de, Junior DM, Toledo SPA, Fragoso MCBV. MEN 1 gene is not implicated in adrenal hyperplasia associated with multiple endocrine neoplasia type 1. Resumos. 2006 ;[citado 2024 out. 01 ]
Vancouver
Costa MHS, Pinto EM, Billerbeck AE, Mendonça BB de, Junior DM, Toledo SPA, Fragoso MCBV. MEN 1 gene is not implicated in adrenal hyperplasia associated with multiple endocrine neoplasia type 1. Resumos. 2006 ;[citado 2024 out. 01 ]
Artigo de periodico
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene (2001)
Ianakiev, P.; Baren, M. J. van; Daly, M. J.; Toledo, S. P. A.; Cavalcanti, M. G.; Correa Neto, J.; Silveira, E. Lemos; Freire Maia, A.; Heutink, P.; Kilpatrick, M. W.; Tsipouras, P.
Fonte: American Journal of Human Genetics. Unidade: FM
Assunto: GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
IANAKIEV, P. et al. Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene. American Journal of Human Genetics, v. 68, p. 38-45, 2001Tradução . . Acesso em: 01 out. 2024.
APA
Ianakiev, P., Baren, M. J. van, Daly, M. J., Toledo, S. P. A., Cavalcanti, M. G., Correa Neto, J., et al. (2001). Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene. American Journal of Human Genetics, 68, 38-45.
NLM
Ianakiev P, Baren MJ van, Daly MJ, Toledo SPA, Cavalcanti MG, Correa Neto J, Silveira EL, Freire Maia A, Heutink P, Kilpatrick MW, Tsipouras P. Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene. American Journal of Human Genetics. 2001 ; 68 38-45.[citado 2024 out. 01 ]
Vancouver
Ianakiev P, Baren MJ van, Daly MJ, Toledo SPA, Cavalcanti MG, Correa Neto J, Silveira EL, Freire Maia A, Heutink P, Kilpatrick MW, Tsipouras P. Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene. American Journal of Human Genetics. 2001 ; 68 38-45.[citado 2024 out. 01 ]

Unidades USP

ReP

Filtros

Autores

Assuntos