Large fetal goiter in a patient with congenital hypothyroidism is associated with intron donor site mutation (G.IVS30+1G>T) of the thyroglobulin gene (2006)
- Authors:
- Autor USP: MEDEIROS NETO, GERALDO ANTONIO DE - FM
- Unidade: FM
- Subjects: HIPOTIREOIDISMO; MUTAÇÃO GENÉTICA; BIOQUÍMICA; HORMÔNIOS TIREOIDIANOS; BIOLOGIA MOLECULAR; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Conference titles: Annual Meeting on the American Thyroid Association
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ABNT
POSSATO, R. et al. Large fetal goiter in a patient with congenital hypothyroidism is associated with intron donor site mutation (G.IVS30+1G>T) of the thyroglobulin gene. 2006, Anais.. New York: Faculdade de Medicina, Universidade de São Paulo, 2006. p. 906. Disponível em: http://online.liebertpub.com/doi/pdfplus/10.1089/thy.2006.16.857. Acesso em: 19 abr. 2024. -
APA
Possato, R., Rubio, I. G. S., Knobel, M., Oliveira, M. H., Moura, M., Rivolta, C., et al. (2006). Large fetal goiter in a patient with congenital hypothyroidism is associated with intron donor site mutation (G.IVS30+1G>T) of the thyroglobulin gene. In Thyroid (Vol. 16, p. 906). New York: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://online.liebertpub.com/doi/pdfplus/10.1089/thy.2006.16.857 -
NLM
Possato R, Rubio IGS, Knobel M, Oliveira MH, Moura M, Rivolta C, Targovnik HM, Medeiros-Neto G. Large fetal goiter in a patient with congenital hypothyroidism is associated with intron donor site mutation (G.IVS30+1G>T) of the thyroglobulin gene [Internet]. Thyroid. 2006 ; 16( 9): 906.[citado 2024 abr. 19 ] Available from: http://online.liebertpub.com/doi/pdfplus/10.1089/thy.2006.16.857 -
Vancouver
Possato R, Rubio IGS, Knobel M, Oliveira MH, Moura M, Rivolta C, Targovnik HM, Medeiros-Neto G. Large fetal goiter in a patient with congenital hypothyroidism is associated with intron donor site mutation (G.IVS30+1G>T) of the thyroglobulin gene [Internet]. Thyroid. 2006 ; 16( 9): 906.[citado 2024 abr. 19 ] Available from: http://online.liebertpub.com/doi/pdfplus/10.1089/thy.2006.16.857 - Genética molecular do hipotiroidismo congênito
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