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[Clinical and molecular genetic features of cases of isolated hypogonadotropic hypogonadism, associated with defects in GNRHR genes].
Makretskaya NA, Gerasimova MV, Vasilyev EV, Zubkova NA, Kalinchenko NY, Kolodkina AA, Petrov VM, Pogoda TV, Panova AV, Frolova EB, Poliakov AV, Tiulpakov AN. Makretskaya NA, et al. Among authors: petrov vm. Probl Endokrinol (Mosk). 2021 May 1;67(3):62-67. doi: 10.14341/probl12746. Probl Endokrinol (Mosk). 2021. PMID: 34297503 Free PMC article. Russian.
[Hereditary Cushing's syndrome caused by primary bilateral macronodular adrenal hyperplasia due to ARMC5 mutation with concomitant primary hyperparathyroidism: the first known case in Russia].
Mamedova EO, Vasilyev EV, Petrov VM, Izmailova NS, Buryakina SA, Rozhinskaya LY, Tiulpakov AN, Belaya ZE. Mamedova EO, et al. Among authors: petrov vm. Probl Endokrinol (Mosk). 2019 Jun 30;65(2):89-94. doi: 10.14341/probl9712. Probl Endokrinol (Mosk). 2019. PMID: 31271710 Russian.
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