Preclinical diagnosis of testotoxicosis in a boy with in activating mutation of the luteinizing hormone receptor (2006)
- Autores:
- Autor USP: MENDONÇA, BERENICE BILHARINHO DE - FM
- Unidade: FM
- Assuntos: HORMÔNIO LUTEINIZANTE; TESTÍCULO (TOXICIDADE); DIAGNÓSTICO; ADOLESCENTES
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Journal of pediatric endocrnology & metabolism
- ISSN: 0334-018X
- Volume/Número/Paginação/Ano: v. 19, n. 4, p. 541-544, 2006
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ABNT
TELES, Milena et al. Preclinical diagnosis of testotoxicosis in a boy with in activating mutation of the luteinizing hormone receptor. Journal of pediatric endocrnology & metabolism, v. 19, n. 4, p. 541-544, 2006Tradução . . Acesso em: 18 abr. 2024. -
APA
Teles, M., Arnhold, I. J. P., Mendonça, B. B., & Latronico, A. C. (2006). Preclinical diagnosis of testotoxicosis in a boy with in activating mutation of the luteinizing hormone receptor. Journal of pediatric endocrnology & metabolism, 19( 4), 541-544. -
NLM
Teles M, Arnhold IJP, Mendonça BB, Latronico AC. Preclinical diagnosis of testotoxicosis in a boy with in activating mutation of the luteinizing hormone receptor. Journal of pediatric endocrnology & metabolism. 2006 ; 19( 4): 541-544.[citado 2024 abr. 18 ] -
Vancouver
Teles M, Arnhold IJP, Mendonça BB, Latronico AC. Preclinical diagnosis of testotoxicosis in a boy with in activating mutation of the luteinizing hormone receptor. Journal of pediatric endocrnology & metabolism. 2006 ; 19( 4): 541-544.[citado 2024 abr. 18 ] - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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