 | Up a level |
Kang, I.N. and Musa, M. and Harun, F. and Junit, S.M. (2010) Characterization of mutations in the FOXE1 gene in a cohort of unrelated Malaysian patients with congenital hypothyroidism and thyroid dysgenesis. Biochemical Genetics, 48 (1-2). pp. 141-151.
