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2. Assessing the clinical and molecular diagnosis of inherited forms of impaired sensitivity to thyroid hormone from a single tertiary center. Ramos LS; Kizys MML; Kunii IS; Spinola-Castro AM; Nesi-França S; Guerra RA; Camacho CP; Martins JRM; Maciel RMB; Dias-da-Silva MR; Chiamolera MI Endocrine; 2018 Dec; 62(3):628-638. PubMed ID: 30027432 [TBL] [Abstract][Full Text] [Related]
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12. Inhibition of serum protein binding of thyroxine in a hypothyroid patient with familial dysalbuminemic hyperthyroxinemia. Premachandra BN; Wortsman J; Williams IK Clin Biochem; 1996 Feb; 29(1):85-8. PubMed ID: 8929830 [TBL] [Abstract][Full Text] [Related]
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20. Diagnosis of familial dysalbuminemic hyperthyroxinemia and investigation of the nature of the variant albumin. Takamatsu J; Ohsawa N Bull Osaka Med Coll; 1990 Nov; 36(1-2):35-45. PubMed ID: 2135643 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]