Source: Hormone Research in Paediatrics. Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, RECEPTORES, GENÉTICA, ENDOCRINOPATIAS
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CHARMANDARI, Evangelia et al. A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 13 out. 2024. , 2013APA
Charmandari, E., Zhang, M., Silveira, L. G., Chrousos, G. P., Sertedaki, A., Xavier, A. C. L., & Segaloff, D. L. (2013). A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.NLM
Charmandari E, Zhang M, Silveira LG, Chrousos GP, Sertedaki A, Xavier ACL, Segaloff DL. A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties. Hormone Research in Paediatrics. 2013 ; 80 44.[citado 2024 out. 13 ]Vancouver
Charmandari E, Zhang M, Silveira LG, Chrousos GP, Sertedaki A, Xavier ACL, Segaloff DL. A case of Leydig cell hypoplasia associated with two distinct homozygous mutations of the human luteinizing hormone/chorionic gonadotropin receptor that include a novel mutation with unusual functional properties. Hormone Research in Paediatrics. 2013 ; 80 44.[citado 2024 out. 13 ]