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: 11 fev. 2026. -
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 2026 fev. 11 ] -
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 2026 fev. 11 ] - Primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 (HTP/Men 1): Increment of bone mineral density after parathyroidectomy
- Somatotroph pituitary adenoma with acromegaly and autosomal dominant polycystic kidney disease: SSTR5 polymorphism and PKD1 mutation
- AIP ad P27/KIP1 gne vriants are not associated ptuitary aenoma penotypes in a large MEN1 family
- Sindrome hereditária caracterizada por micropênis, hipoandrogenismo e níveis séricos altos de gonadotrofinas devido a distúrbio primário nas células de leydig, associada a testículos de tamanho normal e ausência de ambiguidade genital: uma provável nova entidade clínica
- Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female
- A differential diagnosis of inherited endocrine tumors and their tumor counterparts
- Hugt frequency of hirschprung in a large family C620R-ret mutated family
- Peptide hormone receptor defects leading to abnormal phenotypes
- Hypercalcitoninemia is not pathognomonic of medullary thyroid carcinoma
- Germline Mutation in the Aryl Hydrocarbon Receptor Interacting Protein Gene in Familial Somatotropinoma
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
