Absence of mutations in the entire coding region of FSH receptor in patients with latrogenic ovarian hyperstimulation syndrome (2005)
- Autores:
- Autor USP: MENDONCA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Assuntos: OVÁRIO (FISIOPATOLOGIA); POLIMORFISMO; FERTILIDADE; MUTAÇÃO GENÉTICA
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Program and Abstracts
- Nome do evento: The Endocrine Society's Annual Meeting
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ABNT
ALVA, Catarina B. d et al. Absence of mutations in the entire coding region of FSH receptor in patients with latrogenic ovarian hyperstimulation syndrome. 2005, Anais.. San Diego: Faculdade de Medicina, Universidade de São Paulo, 2005. . Acesso em: 19 abr. 2024. -
APA
Alva, C. B. d, Serafini, P., Motta, E., Kohek, M. F., Latronico, A. C., & Mendonça, B. B. (2005). Absence of mutations in the entire coding region of FSH receptor in patients with latrogenic ovarian hyperstimulation syndrome. In Program and Abstracts. San Diego: Faculdade de Medicina, Universidade de São Paulo. -
NLM
Alva CB d, Serafini P, Motta E, Kohek MF, Latronico AC, Mendonça BB. Absence of mutations in the entire coding region of FSH receptor in patients with latrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2005 ;[citado 2024 abr. 19 ] -
Vancouver
Alva CB d, Serafini P, Motta E, Kohek MF, Latronico AC, Mendonça BB. Absence of mutations in the entire coding region of FSH receptor in patients with latrogenic ovarian hyperstimulation syndrome. Program and Abstracts. 2005 ;[citado 2024 abr. 19 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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