Familial leydig cell hypoplasia (lch) not associated to male pseudohermaphroditism (mph): hcg / lh receptor evaluation and h-y antigen typing (1992)
- Authors:
- USP affiliated authors: MOREIRA FILHO, CARLOS ALBERTO - ICB ; OLIVEIRA FILHO, RICARDO MARTINS DE - ICB ; TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidades: ICB; FM
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Publisher: Endocrine Society
- Publisher place: Bethesda
- Date published: 1992
- Source:
- Título do periódico: Program and Abstracts
- Conference titles: Annual Meeting of the Endocrine Society
-
ABNT
TOLEDO, S. P. A. et al. Familial leydig cell hypoplasia (lch) not associated to male pseudohermaphroditism (mph): hcg / lh receptor evaluation and h-y antigen typing. 1992, Anais.. Bethesda: Endocrine Society, 1992. . Acesso em: 19 abr. 2024. -
APA
Toledo, S. P. A., Oliveira Filho, R. M., Moreira-Filho, C. A., & Charreau, E. H. (1992). Familial leydig cell hypoplasia (lch) not associated to male pseudohermaphroditism (mph): hcg / lh receptor evaluation and h-y antigen typing. In Program and Abstracts. Bethesda: Endocrine Society. -
NLM
Toledo SPA, Oliveira Filho RM, Moreira-Filho CA, Charreau EH. Familial leydig cell hypoplasia (lch) not associated to male pseudohermaphroditism (mph): hcg / lh receptor evaluation and h-y antigen typing. Program and Abstracts. 1992 ;[citado 2024 abr. 19 ] -
Vancouver
Toledo SPA, Oliveira Filho RM, Moreira-Filho CA, Charreau EH. Familial leydig cell hypoplasia (lch) not associated to male pseudohermaphroditism (mph): hcg / lh receptor evaluation and h-y antigen typing. Program and Abstracts. 1992 ;[citado 2024 abr. 19 ] - Carcinoma medular de tireoide
- Sindrome hereditaria caracterizada por micropenis, hipoandrogenismo e niveis sericos altos de gonadotrofinas devido a disturbio primario nas celulas de leydig, associada a testiculos de tamanho normal e ausencia de ambiguidade genital: uma provavel nova entidade clinica
- Inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46, xx female
- Missense mutation in the lh receptor gene causas leydig cell hypoplasia
- 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]
- Screening of RET gene mutations in multiple endocrine neoplasia type-2 using Conformation Sensitive Gel Electrophoresis (CSGE)
- Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1
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