Fonte: Clinical Endocrinology. Unidade: FM
Assuntos: POLIMORFISMO (GENÉTICA), MUTAÇÃO GENÉTICA, RECEPTORES, DNA
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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: 23 ago. 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.xNLM
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 ago. 23 ] Available from: https://doi.org/10.1046/j.0300-0664.2001.01437.xVancouver
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 ago. 23 ] Available from: https://doi.org/10.1046/j.0300-0664.2001.01437.x
