Source: Clinical Endocrinology. Unidade: FM
Subjects: HORMÔNIOS, PUBERDADE
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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: 05 dez. 2025.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.xNLM
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 2025 dez. 05 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01810.xVancouver
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 2025 dez. 05 ] Available from: https://doi.org/10.1046/j.1365-2265.2003.01810.x
