Clinical Endocrinologygoes electronic
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.2001.01365.x/fullpdf
Reference109 articles.
1. Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland.
2. The Spectrum of Thyroid Disorders in an Iodine-Deficient Community: The Pescopagano Survey
3. Genomic DNA Analysis of Thyrotropin Receptor in a Family with Hereditary Hyperthyroidism.
4. Corrigendum
5. Interrelationships between age, thyroid volume, thyroid nodularity, and thyroid function in patients with sporadic nontoxic goiter
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3. Graves’ disease, multinodular goiter and subclinical hyperthyroidism;Annales d'Endocrinologie;2019-09
4. A case of congenital autonomous thyroid adenoma with a somatic activating gene mutation in the thyroid-stimulating hormone receptor;Journal of Pediatric Surgery Case Reports;2018-11
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