Source: Journal of Clinical Endocrinology & Metabolism. Unidade: FM
Subjects: ENDOCRINOPATIAS, ENDOCRINOLOGIA
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KOPP, P. et al. Phenocopies for deafness and Goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene. Journal of Clinical Endocrinology & Metabolism, v. 84, n. 1, p. 336-341, 1999Tradução . . Acesso em: 30 set. 2024.APA
Kopp, P., Arseven, O. K., Sabacan, L., Kotlar, T., Dupuis, J., Cavalieri, H., et al. (1999). Phenocopies for deafness and Goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene. Journal of Clinical Endocrinology & Metabolism, 84( 1), 336-341.NLM
Kopp P, Arseven OK, Sabacan L, Kotlar T, Dupuis J, Cavalieri H, Santos CLS, Jameson JL, Medeiros Neto GA. Phenocopies for deafness and Goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene. Journal of Clinical Endocrinology & Metabolism. 1999 ; 84( 1): 336-341.[citado 2024 set. 30 ]Vancouver
Kopp P, Arseven OK, Sabacan L, Kotlar T, Dupuis J, Cavalieri H, Santos CLS, Jameson JL, Medeiros Neto GA. Phenocopies for deafness and Goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene. Journal of Clinical Endocrinology & Metabolism. 1999 ; 84( 1): 336-341.[citado 2024 set. 30 ]