Hypopituitarism Due to Mutation in the PROP1 Gene in Association With the 47,XYY Karyotype and Autosomal Dominant Atrioventricular Septal Defect: Two Case Reports
Problemy Endokrinologii - Russian Federation
doi 10.14341/probl2017633174-178
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Date
June 15, 2017
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Endocrinology Research Centre