A homozygous mutation in the luteinizing hormone receptor causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype (1998)
- Authors:
- USP affiliated authors: ABELIN, NEUSA MARIA ALVES - FM ; TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- Assunto: MEDICINA INTERNA
- Language: Inglês
- Source:
- Título: Molecular Endocrinology
- Volume/Número/Paginação/Ano: v. 12, n. 6, p. 775-784, 1998
-
ABNT
MARTENS, John W. M et al. A homozygous mutation in the luteinizing hormone receptor causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype. Molecular Endocrinology, v. 12, n. 6, p. 775-784, 1998Tradução . . Acesso em: 22 fev. 2026. -
APA
Martens, J. W. M., Post, M. V., Abelin, N. M. A., Ezabella, M. C. L., Toledo, S. P. de A., Brunner, H. G., & Themmen, A. P. N. (1998). A homozygous mutation in the luteinizing hormone receptor causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype. Molecular Endocrinology, 12( 6), 775-784. -
NLM
Martens JWM, Post MV, Abelin NMA, Ezabella MCL, Toledo SP de A, Brunner HG, Themmen APN. A homozygous mutation in the luteinizing hormone receptor causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype. Molecular Endocrinology. 1998 ; 12( 6): 775-784.[citado 2026 fev. 22 ] -
Vancouver
Martens JWM, Post MV, Abelin NMA, Ezabella MCL, Toledo SP de A, Brunner HG, Themmen APN. A homozygous mutation in the luteinizing hormone receptor causes partial leydig cell hypoplasia: correlation between receptor activity and phenotype. Molecular Endocrinology. 1998 ; 12( 6): 775-784.[citado 2026 fev. 22 ] - Diagnosis of medullary carcinoma of the thyroid (mtc) using calcitonin (ct) policlonal radioimmunoassay: criteria for the normal values and pathological levels
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