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Trabalho de evento-resumo
Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty (2004)
Brito, V.; Mendonca, B. B.; Freitas, k.; Arnhold, I.; Latronico, A. C.
Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: HORMÔNIO DO CRESCIMENTO (FISIOPATOLOGIA), PUBERDADE PRECOCE, POLIMORFISMO, GENES SUPRESSORES DE TUMOR (METABOLISMO), GONADOTROFINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRITO, V. et al. Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 31 out. 2024.
APA
Brito, V., Mendonca, B. B., Freitas, k., Arnhold, I., & Latronico, A. C. (2004). Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Brito V, Mendonca BB, Freitas k., Arnhold I, Latronico AC. Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. Program and Abstracts. 2004 ;[citado 2024 out. 31 ]
Vancouver
Brito V, Mendonca BB, Freitas k., Arnhold I, Latronico AC. Mutational analysis of the gaba-a receptor alpha1 subunit gene (gabra 1) in girls familial and sporadic idiophatic gonadotrpin-dependent precocious puberty. Program and Abstracts. 2004 ;[citado 2024 out. 31 ]
Trabalho de evento-resumo
The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect (2004)
Pinto, E. M.; Billerbeck, A. E.; Mendonca, B. B.; Latronico, A. C.
Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: BIOMARCADORES, MUTAÇÃO GENÉTICA, POLIMORFISMO, GENES SUPRESSORES DE TUMOR, BRASILEIROS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINTO, E. M. et al. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 31 out. 2024.
APA
Pinto, E. M., Billerbeck, A. E., Mendonca, B. B., & Latronico, A. C. (2004). The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
Pinto EM, Billerbeck AE, Mendonca BB, Latronico AC. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. Program and Abstracts. 2004 ;[citado 2024 out. 31 ]
Vancouver
Pinto EM, Billerbeck AE, Mendonca BB, Latronico AC. The unusually high incidence of germline Arg337His mutation in the p53 tumor suppressor gene among brazilian with adrenocortical tumors can be attributed to founder effect. Program and Abstracts. 2004 ;[citado 2024 out. 31 ]
Trabalho de evento-resumo
Absence of FSHR activating mutations in women with iatrogenic ovarian hyperstimulation syndrome (2004)
d' Alva, C.; Serafini, P.; Motta, E.; Kohek, M.; Latronico, A.; Mendonca, B. B.
Source: Program and Abstracts. Conference titles: International Congress of Endocrinology. Unidade: FM
Subjects: FERTILIZAÇÃO "IN VITRO" (COMPLICAÇÕES), CISTOS OVARIANOS (COMPLICAÇÕES), OVULAÇÃO (TÉCNICAS), POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
D' ALVA, C. et al. Absence of FSHR activating mutations in women with iatrogenic ovarian hyperstimulation syndrome. 2004, Anais.. Lisboa: International Society of Endocrinology, 2004. . Acesso em: 31 out. 2024.
APA
d' Alva, C., Serafini, P., Motta, E., Kohek, M., Latronico, A., & Mendonca, B. B. (2004). Absence of FSHR activating mutations in women with iatrogenic ovarian hyperstimulation syndrome. In Program and Abstracts. Lisboa: International Society of Endocrinology.
NLM
d' Alva C, Serafini P, Motta E, Kohek M, Latronico A, Mendonca BB. Absence of FSHR activating mutations in women with iatrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2024 out. 31 ]
Vancouver
d' Alva C, Serafini P, Motta E, Kohek M, Latronico A, Mendonca BB. Absence of FSHR activating mutations in women with iatrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2004 ;[citado 2024 out. 31 ]

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