Molecular analysis of p53 vhl and ret genes in pheochromocytoma (1995)
- Autores:
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- Assunto: ENDOCRINOLOGIA
- Idioma: Inglês
- Imprenta:
- Editora: Endocrine Society
- Local: Rockville
- Data de publicação: 1995
- Fonte:
- Título do periódico: Program and Abstracts
- Nome do evento: Annual Meeting of the Endocrine Society
-
ABNT
DAHIA, P L M et al. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. 1995, Anais.. Rockville: Endocrine Society, 1995. . Acesso em: 19 set. 2024. -
APA
Dahia, P. L. M., Aguiar, R. C. T., Eng, C., Crossey, P. A., Maher, E. R., Grossman, A., et al. (1995). Molecular analysis of p53 vhl and ret genes in pheochromocytoma. In Program and Abstracts. Rockville: Endocrine Society. -
NLM
Dahia PLM, Aguiar RCT, Eng C, Crossey PA, Maher ER, Grossman A, Ponder BAJ, Toledo SPA. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. Program and Abstracts. 1995 ;[citado 2024 set. 19 ] -
Vancouver
Dahia PLM, Aguiar RCT, Eng C, Crossey PA, Maher ER, Grossman A, Ponder BAJ, Toledo SPA. Molecular analysis of p53 vhl and ret genes in pheochromocytoma. Program and Abstracts. 1995 ;[citado 2024 set. 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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