Source: Thyroid. Conference titles: International Thyroid Congress. Unidade: FM
Subjects: DIAGNÓSTICO HISTOLÓGICO (MÉTODOS), HIPOTIREOIDISMO, RECÉM-NASCIDO, MUTAÇÃO GENÉTICA (COMPLICAÇÕES), RESUMOS (EVENTOS)
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ABNT
NEVES, S. C. et al. Molecular diagnosis of congenital hypothyroidism with total or partial iodide organification defect, screening for TPO mutations. Thyroid. New York: American Thyroid Association. Disponível em: http://online.liebertpub.com/doi/pdfplus/10.1089/thy.2005.15.s-1. Acesso em: 21 maio 2024. , 2005APA
Neves, S. C., Rubio, I. G. S., Knobel, M., Monteiro, M. S., Pardo, V. L., Galrão, A. L., et al. (2005). Molecular diagnosis of congenital hypothyroidism with total or partial iodide organification defect, screening for TPO mutations. Thyroid. New York: American Thyroid Association. Recuperado de http://online.liebertpub.com/doi/pdfplus/10.1089/thy.2005.15.s-1NLM
Neves SC, Rubio IGS, Knobel M, Monteiro MS, Pardo VL, Galrão AL, Dias V, Viana M, Chagas AJ, Medeiros-Neto GERALDO. Molecular diagnosis of congenital hypothyroidism with total or partial iodide organification defect, screening for TPO mutations [Internet]. Thyroid. 2005 ; 15 S-228.[citado 2024 maio 21 ] Available from: http://online.liebertpub.com/doi/pdfplus/10.1089/thy.2005.15.s-1Vancouver
Neves SC, Rubio IGS, Knobel M, Monteiro MS, Pardo VL, Galrão AL, Dias V, Viana M, Chagas AJ, Medeiros-Neto GERALDO. Molecular diagnosis of congenital hypothyroidism with total or partial iodide organification defect, screening for TPO mutations [Internet]. Thyroid. 2005 ; 15 S-228.[citado 2024 maio 21 ] Available from: http://online.liebertpub.com/doi/pdfplus/10.1089/thy.2005.15.s-1