R M Couch, H J Dean, J S Winter. Show Affiliations »
Abstract
Entities: Chemical Disease Gene Mutation
Mesh: See more » Biological Transport, ActiveCongenital HypothyroidismFemaleHumansHypothyroidism/geneticsHypothyroidism/metabolismInfantInfant, NewbornIodides/metabolismMetabolism, Inborn Errors/etiologyPedigreeThyroid Function TestsThyrotropin/metabolismThyroxine/metabolism
Substances: See more » IodidesThyrotropinThyroxine
Year: 1985 PMID: 3998954 DOI: 10.1016/s0022-3476(85)80249-3
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406