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Filtros : "Fragoso, Maria Candida B. Villares" Limpar

Filtros

USP affiliated authors
- mendonca, berenice bilharinho de (~1)
- mendonça, berenice bilharinho de (~1)
- rocha, manoel de souza (~1)
- zerbini, maria claudia nogueira (~1)
Date published
- 2014 (~1)
- 2005 (~1)
Subjects
- mutação genética (2)
- cromossomos humanos (1)
- hiperplasia suprarrenal congênita (1)
- neoplasias das glândulas (1)
- neoplasias das glândulas suprarrenais (1)

Artigo de periodico
ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia (2014)
Alencar, Guilherme Asmar; Lerario, Antonio Marcondes; Nishi, Mirian Yumie; Mariani, Beatriz Marinho de Paula; Almeida, Madson Queiroz; Tremblay, Johanne; Hamet, Pavel; Zerbini, Maria Claudis Nogueira; Gomes, Gilberto Carlos; Bordeau, Isabelle; Pereira, Maria Adelaide Albergaria; Rocha, Manoel de Souza; Chambo, Jose Carlos; Lacroix, Andre; Mendonça, Berenice Bilharinho; Fragoso, Maria Candida B. Villares
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: POLIMORFISMO, MUTAÇÃO GENÉTICA, HIPERPLASIA SUPRARRENAL CONGÊNITA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALENCAR, Guilherme Asmar et al. ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, v. 99, n. 8, p. E1501-E1509, 2014Tradução . . Disponível em: https://doi.org/10.1210/jc.2013-4237. Acesso em: 04 nov. 2024.
APA
Alencar, G. A., Lerario, A. M., Nishi, M. Y., Mariani, B. M. de P., Almeida, M. Q., Tremblay, J., et al. (2014). ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, 99( 8), E1501-E1509. doi:10.1210/jc.2013-4237
NLM
Alencar GA, Lerario AM, Nishi MY, Mariani BM de P, Almeida MQ, Tremblay J, Hamet P, Zerbini MCN, Gomes GC, Bordeau I, Pereira MAA, Rocha M de S, Chambo JC, Lacroix A, Mendonça BB, Fragoso MCBV. ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 8): E1501-E1509.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1210/jc.2013-4237
Vancouver
Alencar GA, Lerario AM, Nishi MY, Mariani BM de P, Almeida MQ, Tremblay J, Hamet P, Zerbini MCN, Gomes GC, Bordeau I, Pereira MAA, Rocha M de S, Chambo JC, Lacroix A, Mendonça BB, Fragoso MCBV. ARMC5 mutation are a frequent cause of primary macronodular adrenal hyperplasia [Internet]. Journal of Clinical Endocrinology and Metabolism. 2014 ; 99( 8): E1501-E1509.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1210/jc.2013-4237
Artigo de periodico
Deletion mapping of chromosome 17 in benign and malignant adrenocortical tumors associated with the Arg33His mutation of the p53 tumor suppressor protein (2005)
Pinto, Emilia M.; Billerbeck, Ana Elisa C.; Fragoso, Maria Candida B. Villares; Latronico, Ana Claudia; Mendonça, Berenice Bilharinho
Source: Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, CROMOSSOMOS HUMANOS, NEOPLASIAS DAS GLÂNDULAS SUPRARRENAIS, NEOPLASIAS DAS GLÂNDULAS, PROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINTO, Emilia M. et al. Deletion mapping of chromosome 17 in benign and malignant adrenocortical tumors associated with the Arg33His mutation of the p53 tumor suppressor protein. Journal of Clinical Endocrinology & Metabolism, v. 90, n. 5, p. 2976-2981, 2005Tradução . . Acesso em: 04 nov. 2024.
APA
Pinto, E. M., Billerbeck, A. E. C., Fragoso, M. C. B. V., Latronico, A. C., & Mendonça, B. B. (2005). Deletion mapping of chromosome 17 in benign and malignant adrenocortical tumors associated with the Arg33His mutation of the p53 tumor suppressor protein. Journal of Clinical Endocrinology & Metabolism, 90( 5), 2976-2981.
NLM
Pinto EM, Billerbeck AEC, Fragoso MCBV, Latronico AC, Mendonça BB. Deletion mapping of chromosome 17 in benign and malignant adrenocortical tumors associated with the Arg33His mutation of the p53 tumor suppressor protein. Journal of Clinical Endocrinology & Metabolism. 2005 ; 90( 5): 2976-2981.[citado 2024 nov. 04 ]
Vancouver
Pinto EM, Billerbeck AEC, Fragoso MCBV, Latronico AC, Mendonça BB. Deletion mapping of chromosome 17 in benign and malignant adrenocortical tumors associated with the Arg33His mutation of the p53 tumor suppressor protein. Journal of Clinical Endocrinology & Metabolism. 2005 ; 90( 5): 2976-2981.[citado 2024 nov. 04 ]

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