Hypopituitarism due to mutation in the PROP1 gene in association with the 47,XYY karyotype and autosomal dominant atrioventricular septal defect: two case reports

Dilyara N. Gubaeva; Elizaveta M. Orlova; Maria S. Pankratova; Alexander V. Vorontsov; Maria А. Kareva

doi:10.14341/probl8604-6450

For citations:

Gubaeva D.N., Orlova E.M., Pankratova M.S., Vorontsov A.V., Kareva M.А. Hypopituitarism due to mutation in the PROP1 gene in association with the 47,XYY karyotype and autosomal dominant atrioventricular septal defect: two case reports. Problems of Endocrinology. 2017;63(3):174-178. https://doi.org/10.14341/probl2017633174-178

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND 4.0).

ISSN 0375-9660 (Print)
ISSN 2308-1430 (Online)

Username
Password
	Remember me
Not a user? Register with this site Forgot your password?

User

Problems of Endocrinology

For citations:

Cookies policy