Associated Papers
Genetic testing of PAX8 mutations associated with thyroid dysgenesis in Chinese congenital hypothyroidism patients.
Li M et al.
Endokrynologia Polska, 2020
Genetic analysis of the paired box transcription factor (PAX8) gene in a cohort of Polish patients with primary congenital hypothyroidism and dysgenetic thyroid glands.
Kumorowicz-Czoch M et al.
Journal of Pediatric Endocrinology & Metabolism : Jpem, 2015
A De novo PAX8 mutation in a Chinese child with congenital thyroid dysgenesis.
Zou H et al.
International Journal of Clinical and Experimental Pathology, 2015
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