Leydig cell hypoplasia determining familial hypergonadotropic hypogonadism (1985)
- Authors:
- USP affiliated authors: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM ; PAULO HILARIO NASCIMENTO SALDIVA - FM
- Unidade: FM
- Assunto: MUTAÇÃO GENÉTICA
- Language: Português
- Source:
- Título do periódico: Progress in Clinical and Biological Research
- Volume/Número/Paginação/Ano: v.200, p.311-4, 1985
-
ABNT
TOLEDO, S. P. A. et al. Leydig cell hypoplasia determining familial hypergonadotropic hypogonadism. Progress in Clinical and Biological Research, v. 200, p. 311-4, 1985Tradução . . Acesso em: 19 set. 2024. -
APA
Toledo, S. P. A., Arnhold, I. J. P., Luthold, W., Russo, E. M., & Saldiva, P. H. N. (1985). Leydig cell hypoplasia determining familial hypergonadotropic hypogonadism. Progress in Clinical and Biological Research, 200, 311-4. -
NLM
Toledo SPA, Arnhold IJP, Luthold W, Russo EM, Saldiva PHN. Leydig cell hypoplasia determining familial hypergonadotropic hypogonadism. Progress in Clinical and Biological Research. 1985 ;200 311-4.[citado 2024 set. 19 ] -
Vancouver
Toledo SPA, Arnhold IJP, Luthold W, Russo EM, Saldiva PHN. Leydig cell hypoplasia determining familial hypergonadotropic hypogonadism. Progress in Clinical and Biological Research. 1985 ;200 311-4.[citado 2024 set. 19 ] - Clinico - genetic study of leydig cell hypoplasia
- 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)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
