Clinical and molecular genetic features of 3 family cases of the central precocious puberty, due to  MKRN3  gene defects

N. A. Zubkova; A. A. Kolodkina; N. A. Makretskaya; P. L. Okorokov; T. V. Pogoda; E. V. Vasiliev; V. M. Petrov; A. N. Tiulpakov

doi:10.14341/probl12745-9945

For citations:

Zubkova N.A., Kolodkina A.A., Makretskaya N.A., Okorokov P.L., Pogoda T.V., Vasiliev E.V., Petrov V.M., Tiulpakov A.N. Clinical and molecular genetic features of 3 family cases of the central precocious puberty, due to MKRN3 gene defects. Problems of Endocrinology. 2021;67(3):55-61. (In Russ.) https://doi.org/10.14341/probl12745

Views PDF (Rus): 956

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