ABSENT AND DEFECTIVE IODOTYROSINE DEIODINATION IN A FAMILY SOME OF WHOSE MEMBERS ARE GOITROUS CRETINS
- 23 January 1965
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 285 (7378) , 183-185
- https://doi.org/10.1016/s0140-6736(65)90971-2
Abstract
No abstract availableKeywords
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- CONGENITAL DEFECTS IN THE BIOSYNTHESIS OF THYROID HORMONEPublished by American Academy of Pediatrics (AAP) ,1958
- SPORADIC NON-ENDEMIC GOITROUS CRETINISM: IDENTIFICATION AND SIGNIFICANCE OF MONOIODOTYROSINE AND DIIODOTYROSINE IN SERUM AND URINEThe Lancet, 1956
- THE METABOLISM OF IODOTYROSINES. II THE METABOLISM OF MONO- AND DI-IODOTYROSINE II CERTAIN PATIENTS WITH FAMILIAL GOITER*Journal of Clinical Endocrinology & Metabolism, 1956
- SPORADIC NON-ENDEMIC GOITROUS CRETINISM: HEREDITARY TRANSMISSIONThe Lancet, 1956
- THE OCCURRENCE OF MONO- AND DI-IODOTYROSINE IN THE BLOOD OF A PATIENT WITH CONGENITAL GOITER*Journal of Clinical Endocrinology & Metabolism, 1955
- RADIOACTIVE-IODINE STUDIES IN NON-ENDEMIC GOITROUS CRETINISMThe Lancet, 1953