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Bernal Barquero CE, Geysels RC, Jacques V, Carro GH, Martín M, Peyret V, Abregú MC, Papendieck P, Masini-Repiso AM, Savagner F, et al. Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect. International Journal of Molecular Sciences. 2022; 23(16):9251. https://doi.org/10.3390/ijms23169251

Bernal Barquero, Carlos Eduardo, Romina Celeste Geysels, Virginie Jacques, Gerardo Hernán Carro, Mariano Martín, Victoria Peyret, María Celeste Abregú, Patricia Papendieck, Ana María Masini-Repiso, Frédérique Savagner, and et al. 2022. "Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect" International Journal of Molecular Sciences 23, no. 16: 9251. https://doi.org/10.3390/ijms23169251

Bernal Barquero, C. E., Geysels, R. C., Jacques, V., Carro, G. H., Martín, M., Peyret, V., Abregú, M. C., Papendieck, P., Masini-Repiso, A. M., Savagner, F., Chiesa, A. E., Citterio, C. E., & Nicola, J. P. (2022). Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect. International Journal of Molecular Sciences, 23(16), 9251. https://doi.org/10.3390/ijms23169251