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Molecular and Cellular Endocrinology|December 25, 2017
Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidismSofia Siffo, Ezequiela Adrover, Cintia E Citterio, et al.Molecular and Cellular Endocrinology|November 21, 2012
New insights into thyroglobulin gene: molecular analysis of seven novel mutations associated with goiter and hypothyroidismCintia E Citterio, Gloria A Machiavelli, Mirta B Miras, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|July 16, 2014
Clinical and molecular studies related to bone metabolism in patients with congenital adrenal hyperplasiaSilvia Martín, Liliana Muñoz, Adriana Pérez, et al.Endocrine|May 4, 2022
Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesisMaricel F Molina, Patricia Papendieck, Gabriela Sobrero, et al.The Journal of Clinical Endocrinology and Metabolism|April 29, 2021
A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid HormonogenesisMariano Martín, Carlos Pablo Modenutti, Mauco Lucas Gil Rosas, et al.Pageof 2