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Trabalho de evento-resumo
Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors (1995)
Nagai, Maria Aparecida; Medicos, A C; Brentani, Maria Mitzi; Brentani, Ricardo Renzo; Mazoyer, S; Mulligan, L M
Source: Programa e Resumos. Conference titles: Reuniao Anual da Sociedade Brasileira de Bioquimica e Biologia Molecular. Unidade: FM
Assunto: ONCOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAGAI, Maria Aparecida et al. Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors. 1995, Anais.. São Paulo: Sociedade Brasileira de Bioquimica e Biologia Molecular, 1995. . Acesso em: 27 abr. 2024.
APA
Nagai, M. A., Medicos, A. C., Brentani, M. M., Brentani, R. R., Mazoyer, S., & Mulligan, L. M. (1995). Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors. In Programa e Resumos. São Paulo: Sociedade Brasileira de Bioquimica e Biologia Molecular.
NLM
Nagai MA, Medicos AC, Brentani MM, Brentani RR, Mazoyer S, Mulligan LM. Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors. Programa e Resumos. 1995 ;[citado 2024 abr. 27 ]
Vancouver
Nagai MA, Medicos AC, Brentani MM, Brentani RR, Mazoyer S, Mulligan LM. Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors. Programa e Resumos. 1995 ;[citado 2024 abr. 27 ]
Artigo de periodico
Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors (1995)
Nagai, Maria Aparecida; Medeiros, A C; Brentani, Maria Mitzi; Brentani, Ricardo Renzo; Marques, L A; Mazoyer, S; Mulligan, L M
Source: Oncology. Unidade: FM
Assunto: ONCOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAGAI, Maria Aparecida et al. Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors. Oncology, v. no/dec. 1995, n. 6 , p. 448-53, 1995Tradução . . Acesso em: 27 abr. 2024.
APA
Nagai, M. A., Medeiros, A. C., Brentani, M. M., Brentani, R. R., Marques, L. A., Mazoyer, S., & Mulligan, L. M. (1995). Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors. Oncology, no/dec. 1995( 6 ), 448-53.
NLM
Nagai MA, Medeiros AC, Brentani MM, Brentani RR, Marques LA, Mazoyer S, Mulligan LM. Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors. Oncology. 1995 ; no/dec. 1995( 6 ): 448-53.[citado 2024 abr. 27 ]
Vancouver
Nagai MA, Medeiros AC, Brentani MM, Brentani RR, Marques LA, Mazoyer S, Mulligan LM. Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors. Oncology. 1995 ; no/dec. 1995( 6 ): 448-53.[citado 2024 abr. 27 ]
Artigo de periodico
Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas (1995)
Eng, C; Crossey, P A; Mulligan, L M; Healey, C S; Houghton, C; Prowse, A; Chew, S L; Dahia, P L M; Oriordan, J L H; Toledo, S. P. A.; Smith, D P; Maher, E R
Source: Journal of Medical Genetics. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ENG, C et al. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas. Journal of Medical Genetics, v. 32, n. 12, p. 934-7, 1995Tradução . . Disponível em: https://doi.org/10.1136/jmg.32.12.934. Acesso em: 27 abr. 2024.
APA
Eng, C., Crossey, P. A., Mulligan, L. M., Healey, C. S., Houghton, C., Prowse, A., et al. (1995). Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas. Journal of Medical Genetics, 32( 12), 934-7. doi:10.1136/jmg.32.12.934
NLM
Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PLM, Oriordan JLH, Toledo SPA, Smith DP, Maher ER. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas [Internet]. Journal of Medical Genetics. 1995 ;32( 12): 934-7.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1136/jmg.32.12.934
Vancouver
Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PLM, Oriordan JLH, Toledo SPA, Smith DP, Maher ER. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas [Internet]. Journal of Medical Genetics. 1995 ;32( 12): 934-7.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1136/jmg.32.12.934
Artigo de periodico
Allelic loss on distal chromosome 17 p is associated with poor prognosis in a group of brazilian breast cancer patients (1994)
Nagai, Maria Aparecida; Pacheco, M M; Brentani, Maria Mitzi; Marques, L A; Brentani, Ricardo Renzo; Ponder, B A; Mulligan, L M
Source: British Journal of Cancer. Unidade: FM
Assunto: ONCOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAGAI, Maria Aparecida et al. Allelic loss on distal chromosome 17 p is associated with poor prognosis in a group of brazilian breast cancer patients. British Journal of Cancer, v. 69, n. 4 , p. 754-8, 1994Tradução . . Disponível em: https://doi.org/10.1038/bjc.1994.142. Acesso em: 27 abr. 2024.
APA
Nagai, M. A., Pacheco, M. M., Brentani, M. M., Marques, L. A., Brentani, R. R., Ponder, B. A., & Mulligan, L. M. (1994). Allelic loss on distal chromosome 17 p is associated with poor prognosis in a group of brazilian breast cancer patients. British Journal of Cancer, 69( 4 ), 754-8. doi:10.1038/bjc.1994.142
NLM
Nagai MA, Pacheco MM, Brentani MM, Marques LA, Brentani RR, Ponder BA, Mulligan LM. Allelic loss on distal chromosome 17 p is associated with poor prognosis in a group of brazilian breast cancer patients [Internet]. British Journal of Cancer. 1994 ;69( 4 ): 754-8.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1038/bjc.1994.142
Vancouver
Nagai MA, Pacheco MM, Brentani MM, Marques LA, Brentani RR, Ponder BA, Mulligan LM. Allelic loss on distal chromosome 17 p is associated with poor prognosis in a group of brazilian breast cancer patients [Internet]. British Journal of Cancer. 1994 ;69( 4 ): 754-8.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1038/bjc.1994.142
Artigo de periodico
Detailed deletion mapping of chromosome segment 17q12-21 in sporadic breast tumors (1994)
Nagai, Maria Aparecida; Yamamoto, L; Salaorni, S; Pacheco, M M; Brentani, Maria Mitzi; Barbosa, E M; Brentani, Ricardo Renzo; Mazoyer, S; Smith, S A; Ponder, B A J; Mulligan, L M
Source: Genes, Chromosomes & Cancer. Unidade: FM
Assunto: ONCOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAGAI, Maria Aparecida et al. Detailed deletion mapping of chromosome segment 17q12-21 in sporadic breast tumors. Genes, Chromosomes & Cancer, v. 11, p. 58-62, 1994Tradução . . Disponível em: https://doi.org/10.1002/gcc.2870110109. Acesso em: 27 abr. 2024.
APA
Nagai, M. A., Yamamoto, L., Salaorni, S., Pacheco, M. M., Brentani, M. M., Barbosa, E. M., et al. (1994). Detailed deletion mapping of chromosome segment 17q12-21 in sporadic breast tumors. Genes, Chromosomes & Cancer, 11, 58-62. doi:10.1002/gcc.2870110109
NLM
Nagai MA, Yamamoto L, Salaorni S, Pacheco MM, Brentani MM, Barbosa EM, Brentani RR, Mazoyer S, Smith SA, Ponder BAJ, Mulligan LM. Detailed deletion mapping of chromosome segment 17q12-21 in sporadic breast tumors [Internet]. Genes, Chromosomes & Cancer. 1994 ;11 58-62.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/gcc.2870110109
Vancouver
Nagai MA, Yamamoto L, Salaorni S, Pacheco MM, Brentani MM, Barbosa EM, Brentani RR, Mazoyer S, Smith SA, Ponder BAJ, Mulligan LM. Detailed deletion mapping of chromosome segment 17q12-21 in sporadic breast tumors [Internet]. Genes, Chromosomes & Cancer. 1994 ;11 58-62.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1002/gcc.2870110109
Trabalho de evento-resumo
Detailed deletion mapping of chromosome 17q 12-21 in sporadic breast tumours (1994)
Nagai, Maria Aparecida; Yamamoto, L; Salaorni, S; Pacheco, M M; Brentani, Maria Mitzi; Barbosa, E M; Brentani, Ricardo Renzo; Mazoyer, S; Smith, S A; Ponder, B A J; Mulligan, L M
Source: Programa e Resumos. Conference titles: Reuniao Anual da Sociedade Brasileira de Bioquimica e Biologia Molecular. Unidade: FM
Assunto: ONCOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAGAI, Maria Aparecida et al. Detailed deletion mapping of chromosome 17q 12-21 in sporadic breast tumours. 1994, Anais.. São Paulo: Sociedade Brasileira de Bioquimica e Biologia Molecular, 1994. . Acesso em: 27 abr. 2024.
APA
Nagai, M. A., Yamamoto, L., Salaorni, S., Pacheco, M. M., Brentani, M. M., Barbosa, E. M., et al. (1994). Detailed deletion mapping of chromosome 17q 12-21 in sporadic breast tumours. In Programa e Resumos. São Paulo: Sociedade Brasileira de Bioquimica e Biologia Molecular.
NLM
Nagai MA, Yamamoto L, Salaorni S, Pacheco MM, Brentani MM, Barbosa EM, Brentani RR, Mazoyer S, Smith SA, Ponder BAJ, Mulligan LM. Detailed deletion mapping of chromosome 17q 12-21 in sporadic breast tumours. Programa e Resumos. 1994 ;[citado 2024 abr. 27 ]
Vancouver
Nagai MA, Yamamoto L, Salaorni S, Pacheco MM, Brentani MM, Barbosa EM, Brentani RR, Mazoyer S, Smith SA, Ponder BAJ, Mulligan LM. Detailed deletion mapping of chromosome 17q 12-21 in sporadic breast tumours. Programa e Resumos. 1994 ;[citado 2024 abr. 27 ]
Artigo de periodico
Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours (1994)
Eng, C; Smith, D P; Mulligan, L M; Nagai, Maria Aparecida; Healey, C S; Ponder, M A; Gardner, E; Schelimann, G F W; Jackson, C E; Tunnacliffe, A; Ponder, B A J
Source: Human Molecular Genetics. Unidade: FM
Assunto: ONCOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ENG, C et al. Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours. Human Molecular Genetics, v. 3 , n. 2 , p. 237-41, 1994Tradução . . Disponível em: https://doi.org/10.1093/hmg/3.2.237. Acesso em: 27 abr. 2024.
APA
Eng, C., Smith, D. P., Mulligan, L. M., Nagai, M. A., Healey, C. S., Ponder, M. A., et al. (1994). Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours. Human Molecular Genetics, 3 ( 2 ), 237-41. doi:10.1093/hmg/3.2.237
NLM
Eng C, Smith DP, Mulligan LM, Nagai MA, Healey CS, Ponder MA, Gardner E, Schelimann GFW, Jackson CE, Tunnacliffe A, Ponder BAJ. Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours [Internet]. Human Molecular Genetics. 1994 ;3 ( 2 ): 237-41.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1093/hmg/3.2.237
Vancouver
Eng C, Smith DP, Mulligan LM, Nagai MA, Healey CS, Ponder MA, Gardner E, Schelimann GFW, Jackson CE, Tunnacliffe A, Ponder BAJ. Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours [Internet]. Human Molecular Genetics. 1994 ;3 ( 2 ): 237-41.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1093/hmg/3.2.237

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