Human Genome Epidemiology Literature Finder
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Query Trace: Hyperplasia and PROP1[original query] |
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Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD). Clinical endocrinology 2005 Jul 63 (1): 10-8. Turton James P G, Mehta Ameeta, Raza Jamal, Woods Kathryn S, Tiulpakov Anatoly, Cassar Joseph, Chong Kling, Thomas Paul Q, Eunice Marumudi, Ammini Ariachery C, Bouloux Pierre M, Starzyk Jerzy, Hindmarsh Peter C, Dattani Mehul |
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