Records 1 - 2
| Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7.
Journal of endocrinological investigation 2021 Nov .
Acar S, Gürsoy S, Arslan G, Nalbanto?lu Ö, Hazan F, Köprülü Ö, Özkaya B, Özkan
| Somatic Mutations of FOXE1 in Papillary Thyroid Cancer.
Thyroid : official journal of the American Thyroid Association 2015 Aug 25 (8): 904-10.
Mond Michael, Bullock Martyn, Yao Yizhou, Clifton-Bligh Roderick J, Gilfillan Christopher, Fuller Peter