Mutational analysis of the PTH 3'-untranslated region in parathyroid disorders
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.2006.02670.x/fullpdf
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2. Hereditary Hyperferritinemia-Cataract Syndrome Caused by a 29-Base Pair Deletion in the Iron Responsive Element of Ferritin L-Subunit Gene
3. Advances in molecular analysis of fragile X syndrome
4. Molecular Basis of Primary Hyperparathyroidism
5. Hypercalcemia and Ectopic Secretion of Parathyroid Hormone by an Ovarian Carcinoma with Rearrangement of the Gene for Parathyroid Hormone
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Mutational analysis of GCMB, a parathyroid-specific transcription factor, in parathyroid adenoma of primary hyperparathyroidism;Journal of Endocrinology;2011-06-03
2. Molecular Genetics of Parathyroid Disease;World Journal of Surgery;2009-04-17
3. Molecular Alterations in Hereditary and Sporadic Thyroid and Parathyroid Diseases;Advances in Anatomic Pathology;2009-01
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