Skip to contents Koffler, Joachim [Author] Mit-Leid : Geschichte und Problematik eines ethischen Grundwortes Books Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Würzburg: Echter, 2001 Published in: Studien zur systematischen und spirituellen Theologie ; 34 POHLENZ, JOACHIM; SCHÖNBERGER, WINFRIED; KOFFLER, THOMAS; REFETOFF, SAMUEL Resistance to Thyroid Hormone Caused by a New Mutation (V336M) in the Thyroid Hormone Receptor β Gene Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Mary Ann Liebert Inc, 1999 Published in: Thyroid, 9 (1999) 10, Seite 1001-1004 Pohlenz, Joachim; Sadow, Peter M.; Koffler, Thomas; Schönberger, Winfried; Weiss, Roy E.; Refetoff, Samuel Congenital hypothyroidism in a child with unsuspected familial dysalbuminemic hyperthyroxinemia caused by a mutation (R218H) in the human albumin gene Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Elsevier BV, 2001 Published in: The Journal of Pediatrics, 139 (2001) 6, Seite 887-891
Koffler, Joachim [Author] Mit-Leid : Geschichte und Problematik eines ethischen Grundwortes Books Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Würzburg: Echter, 2001 Published in: Studien zur systematischen und spirituellen Theologie ; 34
POHLENZ, JOACHIM; SCHÖNBERGER, WINFRIED; KOFFLER, THOMAS; REFETOFF, SAMUEL Resistance to Thyroid Hormone Caused by a New Mutation (V336M) in the Thyroid Hormone Receptor β Gene Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Mary Ann Liebert Inc, 1999 Published in: Thyroid, 9 (1999) 10, Seite 1001-1004
Pohlenz, Joachim; Sadow, Peter M.; Koffler, Thomas; Schönberger, Winfried; Weiss, Roy E.; Refetoff, Samuel Congenital hypothyroidism in a child with unsuspected familial dysalbuminemic hyperthyroxinemia caused by a mutation (R218H) in the human albumin gene Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Elsevier BV, 2001 Published in: The Journal of Pediatrics, 139 (2001) 6, Seite 887-891
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> Creator Skip to next facet KOFFLER, THOMAS (1) Wert ausschließen Koffler, Joachim (1) Wert ausschließen Koffler, Thomas (1) Wert ausschließen POHLENZ, JOACHIM (1) Wert ausschließen Pohlenz, Joachim (1) Wert ausschließen REFETOFF, SAMUEL (1) Wert ausschließen Refetoff, Samuel (1) Wert ausschließen SCHÖNBERGER, WINFRIED (1) Wert ausschließen Sadow, Peter M. (1) Wert ausschließen Schönberger, Winfried (1) Wert ausschließen Weiss, Roy E. (1) Wert ausschließen Show more show less
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