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Filtros : "Vijlder, Jan J. M. de" Limpar

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Artigo de periodico
A premature stopcodon in thyroglobulin messesger RNA results in familial goiter and moderate hypothyroidism (1999)
Graaf, Simone A. R. Van de; Stalpers, Carrie Ris; Veenboer, Geertruda J. M; Cammenga, Marianne; Santos, Cecilia; Targovnik, Hector M; Vijlder, Jan J. M. de; Medeiros Neto, Geraldo Antônio
Source: The Journal of Endocrinology & Metabolism. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GRAAF, Simone A. R. Van de et al. A premature stopcodon in thyroglobulin messesger RNA results in familial goiter and moderate hypothyroidism. The Journal of Endocrinology & Metabolism, v. 84, n. 07, p. 3537-2542, 1999Tradução . . Acesso em: 20 maio 2024.
APA
Graaf, S. A. R. V. de, Stalpers, C. R., Veenboer, G. J. M., Cammenga, M., Santos, C., Targovnik, H. M., et al. (1999). A premature stopcodon in thyroglobulin messesger RNA results in familial goiter and moderate hypothyroidism. The Journal of Endocrinology & Metabolism, 84( 07), 3537-2542.
NLM
Graaf SARV de, Stalpers CR, Veenboer GJM, Cammenga M, Santos C, Targovnik HM, Vijlder JJM de, Medeiros Neto GA. A premature stopcodon in thyroglobulin messesger RNA results in familial goiter and moderate hypothyroidism. The Journal of Endocrinology & Metabolism. 1999 ; 84( 07): 3537-2542.[citado 2024 maio 20 ]
Vancouver
Graaf SARV de, Stalpers CR, Veenboer GJM, Cammenga M, Santos C, Targovnik HM, Vijlder JJM de, Medeiros Neto GA. A premature stopcodon in thyroglobulin messesger RNA results in familial goiter and moderate hypothyroidism. The Journal of Endocrinology & Metabolism. 1999 ; 84( 07): 3537-2542.[citado 2024 maio 20 ]
Artigo de periodico
A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect (1999)
Santos, Cecilia L. S.; Bikker, Hennie; Rego, Katia G. M.; Nascimento, Antonio C.; Tambascia, Marcos; Vijlder, Jan J. M. de; Medeiros Neto, Geraldo Antônio
Source: Clinical Endocrinology. Unidade: FM
Subjects: ENDOCRINOLOGIA, HORMÔNIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Cecilia L. S. et al. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect. Clinical Endocrinology, v. 51, n. 2, p. 165-172, 1999Tradução . . Disponível em: https://doi.org/10.1046/j.1365-2265.1999.00746.x. Acesso em: 20 maio 2024.
APA
Santos, C. L. S., Bikker, H., Rego, K. G. M., Nascimento, A. C., Tambascia, M., Vijlder, J. J. M. de, & Medeiros Neto, G. A. (1999). A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect. Clinical Endocrinology, 51( 2), 165-172. doi:10.1046/j.1365-2265.1999.00746.x
NLM
Santos CLS, Bikker H, Rego KGM, Nascimento AC, Tambascia M, Vijlder JJM de, Medeiros Neto GA. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect [Internet]. Clinical Endocrinology. 1999 ; 51( 2): 165-172.[citado 2024 maio 20 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00746.x
Vancouver
Santos CLS, Bikker H, Rego KGM, Nascimento AC, Tambascia M, Vijlder JJM de, Medeiros Neto GA. A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect [Internet]. Clinical Endocrinology. 1999 ; 51( 2): 165-172.[citado 2024 maio 20 ] Available from: https://doi.org/10.1046/j.1365-2265.1999.00746.x

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