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pubmed-article:17388795pubmed:abstractTextTo investigate a family with an unusual combination of multiple endocrine neoplasia (MEN1) and the McCune-Albright syndrome for MEN1 mutations and activating GNAS1 mutations at codons Arg201 and Gln227.lld:pubmed
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pubmed-article:17388795pubmed:articleTitleA novel MEN1 intronic mutation associated with multiple endocrine neoplasia type 1.lld:pubmed
pubmed-article:17388795pubmed:affiliationAcademic Endocrine Unit, Nuffield Department of Clinical Medicine, University of Oxford, Oxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, Headington, Oxford OX3 7LJ, UK.lld:pubmed
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