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Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect.
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Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect.
Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect. J Clin Endocrinol Metab. 1998 May; 83(5):1448-54.
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PubMed
subject areas
Alleles
DNA Mutational Analysis
Female
Genotype
Humans
Hyperthyroidism
Immunosorbent Techniques
Infant, Newborn
Mutation
Pedigree
Serum Albumin
Thailand
Thyroxine
Triiodothyronine
authors with profiles
Samuel Refetoff