Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty (2003)
- Authors:
- USP affiliated authors: MENDONCA, BERENICE BILHARINHO DE - FM ; XAVIER, ANA CLAUDIA LATRONICO - FM ; ARNHOLD, IVO JORGE PRADO - FM
- Unidade: FM
- DOI: 10.1046/j.1365-2265.2003.01810.x
- Subjects: HORMÔNIOS; PUBERDADE
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Clinical Endocrinology
- Volume/Número/Paginação/Ano: v. 59, p. 533-534, 2003
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
XAVIER, Ana Claudia Latronico et al. Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty. Clinical Endocrinology, v. 59, p. 533-534, 2003Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.2003.01810.x. Acesso em: 19 abr. 2024. -
APA
Xavier, A. C. L., Billerbeck, A. E. C., Pinto, E. M., d'Alva, C. B., Arnhold, I. J. P., & Mendonça, B. B. (2003). Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty. Clinical Endocrinology, 59, 533-534. doi:10.1046/j.1365-2265.2003.01810.x -
NLM
Xavier ACL, Billerbeck AEC, Pinto EM, d'Alva CB, Arnhold IJP, Mendonça BB. Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty [Internet]. Clinical Endocrinology. 2003 ; 59 533-534.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01810.x -
Vancouver
Xavier ACL, Billerbeck AEC, Pinto EM, d'Alva CB, Arnhold IJP, Mendonça BB. Maternal isodisomy causing homozygosity for a dominant activating mutation of the luteinizing hormone receptor gene in a boy with familial male-limited precocius puberty [Internet]. Clinical Endocrinology. 2003 ; 59 533-534.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01810.x - Variable ACTH-stimulated 17-Hydroxyprogesterone values in 21-hydroxylase deficiency carriers are not related to the different CYP21 gene mutations
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Informações sobre o DOI: 10.1046/j.1365-2265.2003.01810.x (Fonte: oaDOI API)
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