Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas (1995)
- Authors:
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- DOI: 10.1136/jmg.32.12.934
- Assunto: ENDOCRINOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v.32, n.12, p.934-7, dec. 1995
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
ENG, C et al. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas. Journal of Medical Genetics, v. 32, n. 12, p. 934-7, 1995Tradução . . Disponível em: https://doi.org/10.1136/jmg.32.12.934. Acesso em: 09 maio 2024. -
APA
Eng, C., Crossey, P. A., Mulligan, L. M., Healey, C. S., Houghton, C., Prowse, A., et al. (1995). Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas. Journal of Medical Genetics, 32( 12), 934-7. doi:10.1136/jmg.32.12.934 -
NLM
Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PLM, Oriordan JLH, Toledo SPA, Smith DP, Maher ER. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas [Internet]. Journal of Medical Genetics. 1995 ;32( 12): 934-7.[citado 2024 maio 09 ] Available from: https://doi.org/10.1136/jmg.32.12.934 -
Vancouver
Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PLM, Oriordan JLH, Toledo SPA, Smith DP, Maher ER. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas [Internet]. Journal of Medical Genetics. 1995 ;32( 12): 934-7.[citado 2024 maio 09 ] Available from: https://doi.org/10.1136/jmg.32.12.934 - 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
Informações sobre o DOI: 10.1136/jmg.32.12.934 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
