Severe Congenital Hypothyroidism Due to a Homozygous Mutation of the βTSH Gene
- 1 August 1999
- journal article
- case report
- Published by Springer Nature in Pediatric Research
- Vol. 46 (2) , 170-173
- https://doi.org/10.1203/00006450-199908000-00007
Abstract
No abstract availableKeywords
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