Predictive factors for the diagnosis of permanent congenital hypothyroidism and its temporal changes in Sergipe, Brazil – A real-life retrospective study
Author:
Publisher
Archives of Endocrinology and Metabolism
Subject
Endocrinology, Diabetes and Metabolism
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2. DUOX defects and their roles in congenital hypothyroidism;De Deken;Methods Mol Biol,2019
3. Mutation screening of DUOX2 in Chinese patients with congenital hypothyroidism;Fu;J Endocrinol Invest,2015
4. DUOX2/DUOXA2 mutation frequently cause congenital hypothyroidism that evades detection on newborn screening in the united kingdom;Peters;Thyroid,2019
5. Transient versus Permanent Congenital Hypothyroidism after the Age of 3 Years in Infants Detected on the First versus Second Newborn Screening Test in Oregon, USA;Ford;Horm Res Paediatr,2016
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