Identification of novel men1 germline mutations and genetic screening in brazilian families with multiple endocrine neoplasia type (2007)
- Authors:
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- Subjects: MUTAÇÃO GENÉTICA; NEOPLASIAS; ENDOCRINOPATIAS (GENÉTICA)
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Abstracts
- Conference titles: Reunião Anual da Federação de Sociedades de Biologia Experimental(FeSBE)
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ABNT
TOLEDO, R. A. et al. Identification of novel men1 germline mutations and genetic screening in brazilian families with multiple endocrine neoplasia type. 2007, Anais.. São Paulo: FeSBE, 2007. Disponível em: http://www.fesbe.org.br/fesbev4/sistema/static/52/29.007.html. Acesso em: 19 abr. 2024. -
APA
Toledo, R. A., Lourenço Junior, D. M., Coutinho, F. L., & Toledo, S. P. A. (2007). Identification of novel men1 germline mutations and genetic screening in brazilian families with multiple endocrine neoplasia type. In Abstracts. São Paulo: FeSBE. Recuperado de http://www.fesbe.org.br/fesbev4/sistema/static/52/29.007.html -
NLM
Toledo RA, Lourenço Junior DM, Coutinho FL, Toledo SPA. Identification of novel men1 germline mutations and genetic screening in brazilian families with multiple endocrine neoplasia type [Internet]. Abstracts. 2007 ;[citado 2024 abr. 19 ] Available from: http://www.fesbe.org.br/fesbev4/sistema/static/52/29.007.html -
Vancouver
Toledo RA, Lourenço Junior DM, Coutinho FL, Toledo SPA. Identification of novel men1 germline mutations and genetic screening in brazilian families with multiple endocrine neoplasia type [Internet]. Abstracts. 2007 ;[citado 2024 abr. 19 ] Available from: http://www.fesbe.org.br/fesbev4/sistema/static/52/29.007.html - 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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