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Article
Sequence of the variant thyroxine-binding globulin (TBG) in a Montreal family with partial TBG deficiency
The variant thyroxine-binding globulin in a family from Montreal (TBG-M) has a reduced affinity for thyroxine, shows a slight cathodal shift on isoelectric focusing, and has an increased susceptibility to inac...
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Article
Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1
Permanent congenital hypothyroidism is the most prevalent inborn endocrine disorder, and principally due to developmental defects leading to absent, ectopic or hypoplastic thyroid gland. Although commonly rega...