Thyroid Hemiagenesis: Incidence, Clinical Significance, and Genetic Background

Author:

Szczepanek-Parulska Ewelina1,Zybek-Kocik Ariadna1,Wartofsky Leonard2,Ruchała Marek1

Affiliation:

1. Department of Endocrinology, Metabolism and Internal Medicine, Poznan University of Medical Sciences, 60-355 Poznan, Poland

2. Department of Medicine, Washington Hospital Center, Washington, District of Columbia 20010

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference132 articles.

1. PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations;Trueba;J Clin Endocrinol Metab,2005

2. Genetics of congenital hypothyroidism;Park;J Med Genet,2005

3. The role of Hoxa-3 in mouse thymus and thyroid development;Manley;Development,1995

4. The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning;Fagman;Hum Mol Genet,2007

5. Molecular mechanisms of thyroid dysgenesis;Polak;Horm Res,2004

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