Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female (1996)
- Authors:
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of Clinical Endocrinology and Metabolism
- Volume/Número/Paginação/Ano: v.81, n.11, p.3850-4, nov. 1996
-
ABNT
TOLEDO, S. P. A. et al. Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female. Journal of Clinical Endocrinology and Metabolism, v. no 1996, n. 11, p. 3850-4, 1996Tradução . . Acesso em: 12 nov. 2025. -
APA
Toledo, S. P. A., Bunner, H. G., Kraaij, R., Post, M., Dahia, P. L. M., Hayashida, C. Y., et al. (1996). Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female. Journal of Clinical Endocrinology and Metabolism, no 1996( 11), 3850-4. -
NLM
Toledo SPA, Bunner HG, Kraaij R, Post M, Dahia PLM, Hayashida CY, Kremer H, Themmen APN. Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female. Journal of Clinical Endocrinology and Metabolism. 1996 ; no 1996( 11): 3850-4.[citado 2025 nov. 12 ] -
Vancouver
Toledo SPA, Bunner HG, Kraaij R, Post M, Dahia PLM, Hayashida CY, Kremer H, Themmen APN. Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female. Journal of Clinical Endocrinology and Metabolism. 1996 ; no 1996( 11): 3850-4.[citado 2025 nov. 12 ] - Primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 (HPT/MEN1): Increment of bone mineral density after parathyroidectomy
- Neoplasia endócrina múltipla tipo 1
- Niveis de calcitonina em cultura de tecido de carcinoma medular de tireoide
- Mutation analysis of glial cell line-derived neurotrophic factor (GDNF), a ligand for the RET/GDNF receptor alpha complex, in sporadic Phaeochromocytomas
- Evaluation of gonadal function in 107 intersex patients by means of serum antimullerian hormone measurement
- Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene
- Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene
- Function of prolactin and GH-secreting cells patient with inactivating mutations in PIT-1 and PROP-1 genes as assessed by ultrasensitive eias
- Tumor secretor de LH: um novo fenótipo na neoplasia endócrina múltipla tipo 1 (NEM-1)
- Hiperparatireoidismo assintomático (HPTA) na neoplasia endócrina endócrina múltipla tipo 1 (NEM-1)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas