Familial case of normosmic hypogonadotropic hypogonadism with polydactyly, associated with defect of FGFR1 gene

Maria V. Gerasimova; Natalya U. Kalinchenko; Evgeniy V. Vasiliev; Vasiliy M. Petrov; Anatoly N. Tiulpakov

doi:10.14341/probl8706-7305

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Gerasimova M.V., Kalinchenko N.U., Vasiliev E.V., Petrov V.M., Tiulpakov A.N. Familial case of normosmic hypogonadotropic hypogonadism with polydactyly, associated with defect of FGFR1 gene. Problems of Endocrinology. 2018;64(1):38-41. https://doi.org/10.14341/probl8706

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)

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Problems of Endocrinology

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