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Molecular defects in thyroid dysgenesis

Published:2019-08-27 Issue:1 Volume:97 Page:222-231
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Mio Catia¹^ORCID,Grani Giorgio²^ORCID,Durante Cosimo²,Damante Giuseppe¹³

Affiliation:

1. Department of MedicineUniversity of Udine Udine Italy

2. Department of Translational and Precision MedicineSapienza University of Rome Rome Italy

3. Institute of Medical GeneticsAcademic Hospital “Azienda Sanitaria Universitaria Integrata di Udine” Udine Italy

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13627

Reference86 articles.

1. Morphogenesis of the thyroid gland

2. Morphological abnormalities in children with thyroidal congenital hypothyroidism

3. Improved prognosis in congenital bypothyroidism treated before age three months

4. The role of thyroid hormone in fetal neurodevelopment;Morreale de Escobar G;J Pediatr Endocrinol Metab,2001

5. Genetic causes of congenital hypothyroidism due to dyshormonogenesis

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2. Identification of Eukaryotic Translation Initiation Factor 4B as a Novel Candidate Gene for Congenital Hypothyroidism;The Journal of Clinical Endocrinology & Metabolism;2024-04-24

3. JAG1 Variants Confer Genetic Susceptibility to Thyroid Dysgenesis and Thyroid Dyshormonogenesis in 813 Congenital Hypothyroidism in China;International Journal of General Medicine;2024-03

4. GLIS3 expression in the thyroid gland in relation to TSH signaling and regulation of gene expression;Cellular and Molecular Life Sciences;2024-01-28

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