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Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.
Bradley, K J; Cavaco, B M; Bowl, M R; Harding, B; Cranston, T; Fratter, C; Besser, G M; Conceição Pereira, M; Davie, M W J; Dudley, N; Leite, V; Sadler, G P; Seller, A; Thakker, R V.
Affiliation
  • Bradley KJ; Academic Endocrine Unit, Nuffield Department of Clinical Medicine, University of Oxford, Oxford Centre for Diabetes, Endocrinology and Metabolism, OCDEM, Churchill Hospital, Headington, Oxford OX3 7LJ, UK.
Clin Endocrinol (Oxf) ; 64(3): 299-306, 2006 Mar.
Article in En | MEDLINE | ID: mdl-16487440
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Collection: 01-internacional Database: MEDLINE Main subject: Parathyroid Neoplasms / Jaw Neoplasms / Tumor Suppressor Proteins / Hyperparathyroidism Limits: Adult / Child / Female / Humans / Male / Middle aged Language: En Journal: Clin Endocrinol (Oxf) Year: 2006 Document type: Article Affiliation country:
Search on Google
Add to My VHL
Print
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Parathyroid Neoplasms / Jaw Neoplasms / Tumor Suppressor Proteins / Hyperparathyroidism Limits: Adult / Child / Female / Humans / Male / Middle aged Language: En Journal: Clin Endocrinol (Oxf) Year: 2006 Document type: Article Affiliation country: