Source: Hormone Research in Paediatrics. Conference titles: Annual meeting of the European Society for Pediatric Endocrinology (ESPE). Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, DISTÚRBIOS DA FUNÇÃO SEXUAL (GENÉTICA), DOENÇAS HEREDITÁRIAS (DIAGNÓSTICO), RESUMOS (EVENTOS)
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SILVA, Thatiana E. et al. A novel heterozygous nonsense mutation (p.K248X) in wilms´ tumor gene (WT1) in a 46,XY patient with Denys-Drash syndrome. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 03 jun. 2024. , 2010APA
Silva, T. E., Santos, M. G., Martin, R. M., Nishi, M. N., Costa, E. E. M. F., Mendonca, B. B., & Domenice, S. (2010). A novel heterozygous nonsense mutation (p.K248X) in wilms´ tumor gene (WT1) in a 46,XY patient with Denys-Drash syndrome. Hormone Research in Paediatrics. Basel: Faculdade de Medicina, Universidade de São Paulo.NLM
Silva TE, Santos MG, Martin RM, Nishi MN, Costa EEMF, Mendonca BB, Domenice S. A novel heterozygous nonsense mutation (p.K248X) in wilms´ tumor gene (WT1) in a 46,XY patient with Denys-Drash syndrome. Hormone Research in Paediatrics. 2010 ; 74( suppl. 3): 207.[citado 2024 jun. 03 ]Vancouver
Silva TE, Santos MG, Martin RM, Nishi MN, Costa EEMF, Mendonca BB, Domenice S. A novel heterozygous nonsense mutation (p.K248X) in wilms´ tumor gene (WT1) in a 46,XY patient with Denys-Drash syndrome. Hormone Research in Paediatrics. 2010 ; 74( suppl. 3): 207.[citado 2024 jun. 03 ]