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dc.contributor.authorHernández-Ramírez, L. C.en
dc.contributor.authorGabrovska, P.en
dc.contributor.authorDénes, J.en
dc.contributor.authorStals, Karenen
dc.contributor.authorTrivellin, G.en
dc.contributor.authorTilley, D.en
dc.contributor.authorFerrau, F.en
dc.contributor.authorEvanson, J.en
dc.contributor.authorEllard, Sianen
dc.contributor.authorGrossman, A. B.en
dc.contributor.authorRoncaroli, F.en
dc.contributor.authorGadelha, M. R.en
dc.contributor.authorKorbonits, M.en
dc.identifier.citationLandscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis in AIP Mutation Carriers. 2015, 100 (9):E1242-54 J. Clin. Endocrinol. Metab.en
dc.description.abstractFamilial isolated pituitary adenoma (FIPA) due to aryl hydrocarbon receptor interacting protein (AIP) gene mutations is an autosomal dominant disease with incomplete penetrance. Clinical screening of apparently unaffected AIP mutation (AIPmut) carriers could identify previously unrecognized disease.en
dc.publisherEndocrine Societyen
dc.rightsArchived with thanks to The Journal of clinical endocrinology and metabolismen
dc.subjectWessex Classification Subject Headings::Oncology. Pathology.::Geneticsen
dc.subjectWessex Classification Subject Headings::Endocrinologyen
dc.titleLandscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis in AIP Mutation Carriers.en
dc.typeJournal Articleen
dc.typeObservational Studyen
dc.typeResearch Support, Non-U.S. Gov'ten
dc.identifier.journalThe Journal of Clinical Endocrinology and Metabolismen
dc.description.noteThis article is freely available via PubMed Central. Click on the 'Additional Link' above to access the full text.en

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