Fonte: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Assuntos: HIPOTIREOIDISMO (CONGÊNITO;GENÉTICA), SEQUENCIAMENTO GENÉTICO, POLIMORFISMO, MUTAÇÃO GENÉTICA, BRASIL
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GUTNISKY, Viviana J. et al. Two distinct compound heterozygous constellation (R277X / IVS34-1G>C and R277X / R1511X) in the thyroglobulin gene in affected individuals of a Brazilian kindred with congenital goiter and defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism, v. 89, n. 2, p. 646-657, 2004Tradução . . Acesso em: 10 nov. 2024.APA
Gutnisky, V. J., Moya, C. M., Rivolta, C. M., Domené, S., Varela, V., Toniolo, J. V., et al. (2004). Two distinct compound heterozygous constellation (R277X / IVS34-1G>C and R277X / R1511X) in the thyroglobulin gene in affected individuals of a Brazilian kindred with congenital goiter and defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism, 89( 2), 646-657.NLM
Gutnisky VJ, Moya CM, Rivolta CM, Domené S, Varela V, Toniolo JV, Medeiros-Neto G, Targovnik HM. Two distinct compound heterozygous constellation (R277X / IVS34-1G>C and R277X / R1511X) in the thyroglobulin gene in affected individuals of a Brazilian kindred with congenital goiter and defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism. 2004 ; 89( 2): 646-657.[citado 2024 nov. 10 ]Vancouver
Gutnisky VJ, Moya CM, Rivolta CM, Domené S, Varela V, Toniolo JV, Medeiros-Neto G, Targovnik HM. Two distinct compound heterozygous constellation (R277X / IVS34-1G>C and R277X / R1511X) in the thyroglobulin gene in affected individuals of a Brazilian kindred with congenital goiter and defective thyroglobulin synthesis. Journal of Clinical Endocrinology and Metabolism. 2004 ; 89( 2): 646-657.[citado 2024 nov. 10 ]
