You can manage bookmarks using lists, please log in to your user account for this.
Media type:
E-Article
Title:
Congenital hypothyroidism in a child with unsuspected familial dysalbuminemic hyperthyroxinemia caused by a mutation (R218H) in the human albumin gene
Contributor:
Pohlenz, Joachim;
Sadow, Peter M.;
Koffler, Thomas;
Schönberger, Winfried;
Weiss, Roy E.;
Refetoff, Samuel
Published:
Elsevier BV, 2001
Published in:
The Journal of Pediatrics, 139 (2001) 6, Seite 887-891