Familial acromegaly
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference37 articles.
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1. A Japanese Family Meeting the Clinical Diagnostic Criteria for MEN1 with a <i>MEN1</i> Variant of Uncertain Significance;Internal Medicine;2023
2. Polymorphisms in MEN1 and DRD2 genes are associated with the occurrence and characteristics of pituitary adenomas;European Journal of Endocrinology;2016-08
3. Síndromes FIPA y significado clínico de las mutaciones del gen AIP;Actualización en neuroendocrinología;2015
4. Familial pituitary tumors;Clinical Neuroendocrinology;2014
5. Familial acromegaly due to aryl hydrocarbon receptor-interacting protein (AIP) gene mutation in a Turkish cohort;Pituitary;2013-06-07
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