Leydig cell hypoplasia:: cases with new mutations, new polymorphisms and cases without mutations in the luteinizing hormone receptor gene (2002)
- Authors:
- Autor USP: TOLEDO, SERGIO PEREIRA DE ALMEIDA - FM
- Unidade: FM
- DOI: 10.1046/j.0300-0664.2001.01437.x
- Subjects: POLIMORFISMO (GENÉTICA); MUTAÇÃO GENÉTICA; RECEPTORES; DNA
- Language: Inglês
- Imprenta:
- Source:
- Título: Clinical Endocrinology
- ISSN: 0300-0664
- Volume/Número/Paginação/Ano: v. 56, p. 103-112, 2002
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
RICHTER-UNRUH, A. et al. Leydig cell hypoplasia:: cases with new mutations, new polymorphisms and cases without mutations in the luteinizing hormone receptor gene. Clinical Endocrinology, v. 56, p. 103-112, 2002Tradução . . Disponível em: https://doi.org/10.1046/j.0300-0664.2001.01437.x. Acesso em: 09 out. 2024. -
APA
Richter-Unruh, A., Martens, J. W. M., Verhoef-Post, M., Wessels, H. T., Kors, W. A., Sinnecker, G. H. G., et al. (2002). Leydig cell hypoplasia:: cases with new mutations, new polymorphisms and cases without mutations in the luteinizing hormone receptor gene. Clinical Endocrinology, 56, 103-112. doi:10.1046/j.0300-0664.2001.01437.x -
NLM
Richter-Unruh A, Martens JWM, Verhoef-Post M, Wessels HT, Kors WA, Sinnecker GHG, Boehmer A, Drop SLS, Toledo SPA, Brunner HG, Themmen APN. Leydig cell hypoplasia:: cases with new mutations, new polymorphisms and cases without mutations in the luteinizing hormone receptor gene [Internet]. Clinical Endocrinology. 2002 ; 56 103-112.[citado 2024 out. 09 ] Available from: https://doi.org/10.1046/j.0300-0664.2001.01437.x -
Vancouver
Richter-Unruh A, Martens JWM, Verhoef-Post M, Wessels HT, Kors WA, Sinnecker GHG, Boehmer A, Drop SLS, Toledo SPA, Brunner HG, Themmen APN. Leydig cell hypoplasia:: cases with new mutations, new polymorphisms and cases without mutations in the luteinizing hormone receptor gene [Internet]. Clinical Endocrinology. 2002 ; 56 103-112.[citado 2024 out. 09 ] Available from: https://doi.org/10.1046/j.0300-0664.2001.01437.x - 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: 10.1046/j.0300-0664.2001.01437.x (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
