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Artigo de periodico
Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency (2014)
Santos, Mariza G.; Machado, Aline Z.; Martins, Conceição N.; Domenice, Sorahia; Mendonça, Berenice B.; Costa, Elaine M. F.; Nishi, Mirian Y.; Ferraz-de-Souza, Bruno; Jorge, Soraia A. C.; Pereira, Carlos A.; Soardi, Fernanda c.; Mello, Maricilda P. de; Maciel-Guerra, Andrea T.; Guerra Junior, Gil
Source: BioMed Research International. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, OVÁRIO (ANORMALIDADES), APOPTOSE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Mariza G. et al. Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency. BioMed Research International, v. 2014, p. 8 art, 2014Tradução . . Disponível em: https://doi.org/10.1155/2014/787465. Acesso em: 01 nov. 2024.
APA
Santos, M. G., Machado, A. Z., Martins, C. N., Domenice, S., Mendonça, B. B., Costa, E. M. F., et al. (2014). Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency. BioMed Research International, 2014, 8 art. doi:10.1155/2014/787465
NLM
Santos MG, Machado AZ, Martins CN, Domenice S, Mendonça BB, Costa EMF, Nishi MY, Ferraz-de-Souza B, Jorge SAC, Pereira CA, Soardi F c., Mello MP de, Maciel-Guerra AT, Guerra Junior G. Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency [Internet]. BioMed Research International. 2014 ; 2014 8 art.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1155/2014/787465
Vancouver
Santos MG, Machado AZ, Martins CN, Domenice S, Mendonça BB, Costa EMF, Nishi MY, Ferraz-de-Souza B, Jorge SAC, Pereira CA, Soardi F c., Mello MP de, Maciel-Guerra AT, Guerra Junior G. Homozygous inactivating mutation in NANOS3 in two sisters with primary ovarian insufficiency [Internet]. BioMed Research International. 2014 ; 2014 8 art.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1155/2014/787465
Artigo de periodico
Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients (2009)
Soardi, Fernanda C.; Penachioni, Junia Y.; Justo, Giselle Z.; Bachega, Tânia A. S. S.; Inácio, Marlene; Mendonça, Berenice Bilharinho de; Castro, Margaret de; Mello, Maricilda P. de
Source: Journal of clinical endocrinology and metabolism. Unidades: FM, FMRP
Subjects: HIDROXILASE (DEFICIÊNCIA), GENES (CLASSIFICAÇÃO), MUTAÇÃO GENÉTICA, FENÓTIPOS, HIPERTENSÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOARDI, Fernanda C. et al. Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism, v. 94, n. 9, p. 3481-3485, 2009Tradução . . Acesso em: 01 nov. 2024.
APA
Soardi, F. C., Penachioni, J. Y., Justo, G. Z., Bachega, T. A. S. S., Inácio, M., Mendonça, B. B. de, et al. (2009). Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism, 94( 9), 3481-3485.
NLM
Soardi FC, Penachioni JY, Justo GZ, Bachega TASS, Inácio M, Mendonça BB de, Castro M de, Mello MP de. Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism. 2009 ; 94( 9): 3481-3485.[citado 2024 nov. 01 ]
Vancouver
Soardi FC, Penachioni JY, Justo GZ, Bachega TASS, Inácio M, Mendonça BB de, Castro M de, Mello MP de. Novel mutations in CYP11B1 gene leading to 11 'beta'-hydroxylase deficiencey in brazilian patients. Journal of clinical endocrinology and metabolism. 2009 ; 94( 9): 3481-3485.[citado 2024 nov. 01 ]
Trabalho de evento-resumo periodico
A novel mutation (G267S) on the CYP11B1 gene in a patient with 11ß-hydroxylase deficiency causing complete virilization (2001)
Mello, Maricilda P. de; Penachioni, Junia Y.; Castro, Margaret de; Bachega, Tania A. S. S.; Mendonca, Berenice Bilharinho
Source: Pediatric Research. Conference titles: Annual Meeting of the Pediatric Academic Societies. Unidade: FM
Subjects: ENDOCRINOLOGIA, BIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MELLO, Maricilda P. de et al. A novel mutation (G267S) on the CYP11B1 gene in a patient with 11ß-hydroxylase deficiency causing complete virilization. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 01 nov. 2024. , 2001
APA
Mello, M. P. de, Penachioni, J. Y., Castro, M. de, Bachega, T. A. S. S., & Mendonca, B. B. (2001). A novel mutation (G267S) on the CYP11B1 gene in a patient with 11ß-hydroxylase deficiency causing complete virilization. Pediatric Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Mello MP de, Penachioni JY, Castro M de, Bachega TASS, Mendonca BB. A novel mutation (G267S) on the CYP11B1 gene in a patient with 11ß-hydroxylase deficiency causing complete virilization. Pediatric Research. 2001 ; 49( 4 pt. 2): 119A. res. PI-711.[citado 2024 nov. 01 ]
Vancouver
Mello MP de, Penachioni JY, Castro M de, Bachega TASS, Mendonca BB. A novel mutation (G267S) on the CYP11B1 gene in a patient with 11ß-hydroxylase deficiency causing complete virilization. Pediatric Research. 2001 ; 49( 4 pt. 2): 119A. res. PI-711.[citado 2024 nov. 01 ]

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