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Artigo de periodico
Inactivating mutations in the LH receptor: as rare as "a hen with teeth" or as frequent as polycystic ovary syndrome? (2000)
Toledo, S. P. A.; Marino, Filomena
Fonte: Fertility & Sterility. Unidade: FM
Assunto: CLÍNICA GERAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TOLEDO, S. P. A. e MARINO, Filomena. Inactivating mutations in the LH receptor: as rare as "a hen with teeth" or as frequent as polycystic ovary syndrome?. Fertility & Sterility, v. 73, p. 655-656, 2000Tradução . . Acesso em: 01 out. 2024.
APA
Toledo, S. P. A., & Marino, F. (2000). Inactivating mutations in the LH receptor: as rare as "a hen with teeth" or as frequent as polycystic ovary syndrome? Fertility & Sterility, 73, 655-656.
NLM
Toledo SPA, Marino F. Inactivating mutations in the LH receptor: as rare as "a hen with teeth" or as frequent as polycystic ovary syndrome? Fertility & Sterility. 2000 ; 73 655-656.[citado 2024 out. 01 ]
Vancouver
Toledo SPA, Marino F. Inactivating mutations in the LH receptor: as rare as "a hen with teeth" or as frequent as polycystic ovary syndrome? Fertility & Sterility. 2000 ; 73 655-656.[citado 2024 out. 01 ]
Artigo de periodico
Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene (2000)
Pernasetti, Flavia; Toledo, S. P. A.; Vasilyev, Vyacheslav V; Hayashida, Cesar Y; Cogan, Joy D; Ferrari, Carmela; Lourenço, Delmar M; Mellon, Pamela L
Fonte: The Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PERNASETTI, Flavia et al. Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene. The Journal of Clinical Endocrinology & Metabolism, v. 85, n. 01, p. 390-397, 2000Tradução . . Acesso em: 01 out. 2024.
APA
Pernasetti, F., Toledo, S. P. A., Vasilyev, V. V., Hayashida, C. Y., Cogan, J. D., Ferrari, C., et al. (2000). Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene. The Journal of Clinical Endocrinology & Metabolism, 85( 01), 390-397.
NLM
Pernasetti F, Toledo SPA, Vasilyev VV, Hayashida CY, Cogan JD, Ferrari C, Lourenço DM, Mellon PL. Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene. The Journal of Clinical Endocrinology & Metabolism. 2000 ; 85( 01): 390-397.[citado 2024 out. 01 ]
Vancouver
Pernasetti F, Toledo SPA, Vasilyev VV, Hayashida CY, Cogan JD, Ferrari C, Lourenço DM, Mellon PL. Impaired adrenocorticotropin-adrenal axis in combined pituytary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene. The Journal of Clinical Endocrinology & Metabolism. 2000 ; 85( 01): 390-397.[citado 2024 out. 01 ]
Artigo de periodico
Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha (2000)
Hayashida, Cesar Yoiti; Gondo, Rogerio G; Ferrari, Carmela; Toledo, S. P. A.; Salvatori, Roberto; Levine, Michael A; Ezabella, Marilza Cristina Legrazie; Abelin, Neusa; Gianella Neto, Daniel; Wajchenberg, Bernardo Leo
Fonte: European Journal of Endocrinology. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HAYASHIDA, Cesar Yoiti et al. Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha. European Journal of Endocrinology, v. 142, n. 06, p. 557-563, 2000Tradução . . Disponível em: https://doi.org/10.1530/eje.0.1420557. Acesso em: 01 out. 2024.
APA
Hayashida, C. Y., Gondo, R. G., Ferrari, C., Toledo, S. P. A., Salvatori, R., Levine, M. A., et al. (2000). Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha. European Journal of Endocrinology, 142( 06), 557-563. doi:10.1530/eje.0.1420557
NLM
Hayashida CY, Gondo RG, Ferrari C, Toledo SPA, Salvatori R, Levine MA, Ezabella MCL, Abelin N, Gianella Neto D, Wajchenberg BL. Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha [Internet]. European Journal of Endocrinology. 2000 ; 142( 06): 557-563.[citado 2024 out. 01 ] Available from: https://doi.org/10.1530/eje.0.1420557
Vancouver
Hayashida CY, Gondo RG, Ferrari C, Toledo SPA, Salvatori R, Levine MA, Ezabella MCL, Abelin N, Gianella Neto D, Wajchenberg BL. Familial growth hormone deficiency with mutated GHRH receptor gene: clinical and hormonal findings in homozygous and heterozygous individuals from Itabaianinha [Internet]. European Journal of Endocrinology. 2000 ; 142( 06): 557-563.[citado 2024 out. 01 ] Available from: https://doi.org/10.1530/eje.0.1420557
Artigo de periodico
Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene (2000)
Ianakiev, P; van Baren, M. J; Daly, M. J; Toledo, S. P. A.; Cavalcanti, M. G; Correia Neto, J; Silveira, E. Lemos; Maia, Ademar Freire; Heutink, P; Kilpatrick, M. W; Tsipouras, P
Fonte: American Journal of Human Genetics. Unidade: FM
Assunto: MEDICINA INTERNA
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. 01-08, 2000Tradução . . Acesso em: 01 out. 2024.
APA
Ianakiev, P., van Baren, M. J., Daly, M. J., Toledo, S. P. A., Cavalcanti, M. G., Correia Neto, J., et al. (2000). Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene. American Journal of Human Genetics, 68, 01-08.
NLM
Ianakiev P, van Baren MJ, Daly MJ, Toledo SPA, Cavalcanti MG, Correia Neto J, Silveira EL, Maia AF, 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. 2000 ; 68 01-08.[citado 2024 out. 01 ]
Vancouver
Ianakiev P, van Baren MJ, Daly MJ, Toledo SPA, Cavalcanti MG, Correia Neto J, Silveira EL, Maia AF, 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. 2000 ; 68 01-08.[citado 2024 out. 01 ]

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