Fonte: Thyroid. Nome do evento: International Thyroid Congress. Unidade: FM
Assuntos: DIAGNÓSTICO HISTOLÓGICO (MÉTODOS), HIPOTIREOIDISMO, RECÉM-NASCIDO, MUTAÇÃO GENÉTICA (COMPLICAÇÕES), RESUMOS (EVENTOS)
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: 30 set. 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 set. 30 ] 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 set. 30 ] Available from: http://online.liebertpub.com/doi/pdfplus/10.1089/thy.2005.15.s-1