Missense mutation in the lh receptor gene causas leydig cell hypoplasia (1995)
- Authors:
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Publisher: Endocrine Society
- Publisher place: Rockville
- Date published: 1995
- Source:
- Título: Program and Abstracts
- Conference titles: Annual Meeting of the Endocrine Society
-
ABNT
THEMMEN, A P N et al. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 27 dez. 2025. -
APA
Themmen, A. P. N., Kraais, R., Kremer, H., Post, M., Toledo, S. P. A., Brunner, H. G., & Grootegoed, J. A. (1995). Missense mutation in the lh receptor gene causas leydig cell hypoplasia. In Program and Abstracts. Rockville: Endocrine Society. -
NLM
Themmen APN, Kraais R, Kremer H, Post M, Toledo SPA, Brunner HG, Grootegoed JA. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. Program and Abstracts. 1995 ;[citado 2025 dez. 27 ] -
Vancouver
Themmen APN, Kraais R, Kremer H, Post M, Toledo SPA, Brunner HG, Grootegoed JA. Missense mutation in the lh receptor gene causas leydig cell hypoplasia. Program and Abstracts. 1995 ;[citado 2025 dez. 27 ] - Carcinoma medular de tireoide
- Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female
- Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutations
- Neoplasias endócrinas múltiplas
- Relato de caso de tireotropinoma
- Germline mutations in TMEM127 confer susceptibility to pheochromocytoma [Carta]
- Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1
- Growth hormone response to growth hormone-releasing peptide-2 in growth hormone-deficient Little mice
- Inactivating mutations of the LH receptor gene: more than two different phenotypes
- Leydig cell hypoplasia:: cases with new mutations, new polymorphisms and cases without mutations in the luteinizing hormone receptor gene
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
