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 (2013)
- Authors:
- Autor USP: XAVIER, ANA CLAUDIA LATRÔNICO - FM
- Unidade: FM
- Subjects: MUTAÇÃO GENÉTICA; RECEPTORES; GENÉTICA; ENDOCRINOPATIAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Hormone Research in Paediatrics
- ISSN: 1663-2818
- Volume/Número/Paginação/Ano: v. 80, suppl. 1, p. 44, res. FC4-164, 2013
- Conference titles: European Society for Paediatric Endocrinology (ESPE)/ Joint Meeting
-
ABNT
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: 01 jun. 2024. , 2013 -
APA
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 jun. 01 ] -
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 jun. 01 ] - Hipogonadismo
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