Developmental Abnormalities of the Thyroid
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Publisher
Elsevier
Reference65 articles.
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1. Novel Mutations in the NKX2.1 gene and the PAX8 gene in a Boy with Brain-Lung-Thyroid Syndrome;Experimental and Clinical Endocrinology & Diabetes;2017-09-27
2. Thyroid function in Down syndrome;Expert Review of Endocrinology & Metabolism;2015-07
3. A New Mutation in the Promoter Region of the PAX8 Gene Causes True Congenital Hypothyroidism with Thyroid Hypoplasia in a Girl with Down's Syndrome;Thyroid;2014-06
4. A New PAX8 Mutation Causing Congenital Hypothyroidism in Three Generations of a Family Is Associated with Abnormalities in the Urogenital Tract;Thyroid;2013-09
5. Two Cases of Thyroid Dysgenesis Caused by Different Novel PAX8 Mutations in the DNA-Binding Region: In Vitro Studies Reveal Different Pathogenic Mechanisms;Thyroid;2013-07
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