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Filtros : "BRASILEIROS" "Gomes, C." Limpar

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Artigo de periodico
Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD) (2007)
Costa, E.; Domenice, S.; Billerbeck, A.; Melo, K.; Correa, R.; Nishi, M.; Pinto, E.; Gomes, C.; Coletta, R.; Abreu, A.; Brandão, M.; Martin, R.; Marui, S.; Xavier, Ana Claudia Latronico; Arnhold, I.; Mendonça, Berenice Bilharinho de
Source: Hormone research. Conference titles: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Subjects: CROMOSSOMOS SEXUAIS (DEFICIÊNCIA), TERAPIA, BRASILEIROS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, E. et al. Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD). Hormone research, v. 68, p. 6, 2007Tradução . . Acesso em: 16 nov. 2024.
APA
Costa, E., Domenice, S., Billerbeck, A., Melo, K., Correa, R., Nishi, M., et al. (2007). Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD). Hormone research, 68, 6.
NLM
Costa E, Domenice S, Billerbeck A, Melo K, Correa R, Nishi M, Pinto E, Gomes C, Coletta R, Abreu A, Brandão M, Martin R, Marui S, Xavier ACL, Arnhold I, Mendonça BB de. Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD). Hormone research. 2007 ; 68 6.[citado 2024 nov. 16 ]
Vancouver
Costa E, Domenice S, Billerbeck A, Melo K, Correa R, Nishi M, Pinto E, Gomes C, Coletta R, Abreu A, Brandão M, Martin R, Marui S, Xavier ACL, Arnhold I, Mendonça BB de. Frequency of molecular diagnosis in brazilian patients with 46,XY disorders of sexual development (DSD). Hormone research. 2007 ; 68 6.[citado 2024 nov. 16 ]
Artigo de periodico
Absence of mutations in DHG gene in brazilian patients with 46,XY disorders of gonadal development (2007)
Gomes, C.; Domenice, S.; Arnhold, I.; Mendonça, Berenice Bilharinho de; Costa, E.
Source: Hormone research. Conference titles: Annual meeting of the sociedad latino-americana de endocrinología pediátrica - SLEP. Unidade: FM
Subjects: BRASILEIROS, TRANSTORNOS DA DIFERENCIAÇÃO SEXUAL, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, C. et al. Absence of mutations in DHG gene in brazilian patients with 46,XY disorders of gonadal development. Hormone research, v. 68, p. 12, 2007Tradução . . Acesso em: 16 nov. 2024.
APA
Gomes, C., Domenice, S., Arnhold, I., Mendonça, B. B. de, & Costa, E. (2007). Absence of mutations in DHG gene in brazilian patients with 46,XY disorders of gonadal development. Hormone research, 68, 12.
NLM
Gomes C, Domenice S, Arnhold I, Mendonça BB de, Costa E. Absence of mutations in DHG gene in brazilian patients with 46,XY disorders of gonadal development. Hormone research. 2007 ; 68 12.[citado 2024 nov. 16 ]
Vancouver
Gomes C, Domenice S, Arnhold I, Mendonça BB de, Costa E. Absence of mutations in DHG gene in brazilian patients with 46,XY disorders of gonadal development. Hormone research. 2007 ; 68 12.[citado 2024 nov. 16 ]

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