Authors: Heinrichs, C Parma, J Scherberg, NH Delange, F Van Vliet, G Duprez, L Bourdoux, P Bergmann, P Vassart, G Refetoff, S

Citation: C. Heinrichs et al., Congenital central isolated hypothyroidism caused by a homozygous mutationin the TSH-beta subunit gene, THYROID, 10(5), 2000, pp. 387-391

Authors: Pannain, S Feldman, M Eiholzer, U Weiss, RE Scherberg, NH Refetoff, S

Citation: S. Pannain et al., Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine, J CLIN END, 85(8), 2000, pp. 2786-2792