Montenegro, Luciana Ribeiro; Seraphim, Carlos; Tinano, Flavia; Piovesan, Maiara; Canton, Ana P. M; Mcelreavey, Ken; Brabant, Severine; Boris, Natalia P.; Magnuson, Melissa; Xavier, Ana Claudia Latronico 
Source: European journal of endocrinology. Unidade: FM
Subjects: PUBERDADE PRECOCE, DOENÇAS HEREDITÁRIAS
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MONTENEGRO, Luciana Ribeiro et al. Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levels. European journal of endocrinology, v. 189, n. 3, p. 422-428, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/57332. Acesso em: 09 nov. 2024.APA
Montenegro, L. R., Seraphim, C., Tinano, F., Piovesan, M., Canton, A. P. M., Mcelreavey, K., et al. (2023). Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levels. European journal of endocrinology, 189( 3), 422-428. doi:10.1093/ejendo/lvad129NLM
Montenegro LR, Seraphim C, Tinano F, Piovesan M, Canton APM, Mcelreavey K, Brabant S, Boris NP, Magnuson M, Xavier ACL. Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levels [Internet]. European journal of endocrinology. 2023 ; 189( 3): 422-428.[citado 2024 nov. 09 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57332Vancouver
Montenegro LR, Seraphim C, Tinano F, Piovesan M, Canton APM, Mcelreavey K, Brabant S, Boris NP, Magnuson M, Xavier ACL. Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levels [Internet]. European journal of endocrinology. 2023 ; 189( 3): 422-428.[citado 2024 nov. 09 ] Available from: https://observatorio.fm.usp.br/handle/OPI/57332
