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NOBOX gene variants in premature ovarian insufficiency: ethnicity-dependent insights.
J Assist Reprod Genet. 2024 Jan;41(1):135-146. doi: 10.1007/s10815-023-02981-y. Epub 2023 Nov 3.
J Assist Reprod Genet. 2024.
PMID: 37921973
Shifting the landscape: Dominant C-terminal rare missense FOXL2 variants in non-syndromic primary ovarian failure etiology.
Jordan P, Verebi C, Hervé B, Perol S, Chakhtoura Z, Courtillot C, Bachelot A, Karila D, Renard C, Grouthier V, de la Croix SM, Bernard V, Fouveaut C, de la Perrière AB, Jonard-Catteau S, Touraine P, Plu-Bureau G, Dupont JM, Christin-Maitre S, Bienvenu T.
Jordan P, et al. Among authors: jonard catteau s.
Clin Genet. 2024 Apr 1. doi: 10.1111/cge.14526. Online ahead of print.
Clin Genet. 2024.
PMID: 38558253
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