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Filtros : "Targovnik, Hector M" Removido: "Stalpers, Carrie Ris" Limpar

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Artigo de periodico
Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a brazilian family with congenital goiter and hypothyroidism (1998)
Targovnik, Hector M; Frechtel, Gustavo D; Mendive, Fernando M; Vono, Jussara; Cochaux, Pascale; Vassart, Gilbert; Medeiros Neto, Geraldo Antônio
Source: Thyroid. Unidade: FM
Assunto: MEDICINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TARGOVNIK, Hector M et al. Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a brazilian family with congenital goiter and hypothyroidism. Thyroid, v. 8, n. 4, p. 291-297, 1998Tradução . . Acesso em: 27 set. 2024.
APA
Targovnik, H. M., Frechtel, G. D., Mendive, F. M., Vono, J., Cochaux, P., Vassart, G., & Medeiros Neto, G. A. (1998). Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a brazilian family with congenital goiter and hypothyroidism. Thyroid, 8( 4), 291-297.
NLM
Targovnik HM, Frechtel GD, Mendive FM, Vono J, Cochaux P, Vassart G, Medeiros Neto GA. Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a brazilian family with congenital goiter and hypothyroidism. Thyroid. 1998 ; 8( 4): 291-297.[citado 2024 set. 27 ]
Vancouver
Targovnik HM, Frechtel GD, Mendive FM, Vono J, Cochaux P, Vassart G, Medeiros Neto GA. Evidence for the segregation of three different mutated alleles of the thyroglobulin gene in a brazilian family with congenital goiter and hypothyroidism. Thyroid. 1998 ; 8( 4): 291-297.[citado 2024 set. 27 ]
Artigo de periodico
Clinical, pathological, and molecular studies of two families with iodide organification defect (1997)
Rego, Katia Garretano de Moraes; Billerbeck, Ana Elisa C; Targovnik, Hector M; Santos, Cecília L S; Alkmin, Maria G; Barbosa, Sonia; Camargo, Rosalina; Medeiros Neto, Geraldo Antônio
Source: Endocrine Pathology. Unidade: FM
Assunto: PATOLOGIA CLÍNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REGO, Katia Garretano de Moraes et al. Clinical, pathological, and molecular studies of two families with iodide organification defect. Endocrine Pathology, v. 8, n. 1, p. 37-47, 1997Tradução . . Disponível em: https://doi.org/10.1007/bf02739706. Acesso em: 27 set. 2024.
APA
Rego, K. G. de M., Billerbeck, A. E. C., Targovnik, H. M., Santos, C. L. S., Alkmin, M. G., Barbosa, S., et al. (1997). Clinical, pathological, and molecular studies of two families with iodide organification defect. Endocrine Pathology, 8( 1), 37-47. doi:10.1007/bf02739706
NLM
Rego KG de M, Billerbeck AEC, Targovnik HM, Santos CLS, Alkmin MG, Barbosa S, Camargo R, Medeiros Neto GA. Clinical, pathological, and molecular studies of two families with iodide organification defect [Internet]. Endocrine Pathology. 1997 ; 8( 1): 37-47.[citado 2024 set. 27 ] Available from: https://doi.org/10.1007/bf02739706
Vancouver
Rego KG de M, Billerbeck AEC, Targovnik HM, Santos CLS, Alkmin MG, Barbosa S, Camargo R, Medeiros Neto GA. Clinical, pathological, and molecular studies of two families with iodide organification defect [Internet]. Endocrine Pathology. 1997 ; 8( 1): 37-47.[citado 2024 set. 27 ] Available from: https://doi.org/10.1007/bf02739706

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