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Items where Author is "Turova, S.V."

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Abaturov, O.E. and Nikulina, A.O. and Yenhovatova, V.А. and Turova, S.V. (2026) Kallmann syndrome type 2 associated with a rare missense mutation in the FGFR1 gene: a clinical case report. Український журнал дитячої ендокринології (1). pp. 23-30. ISSN 2304-005X (Print), 2523-4277 (Online)

This list was generated on Sat Aug 15 02:13:34 2026 EEST.
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