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Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency

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https://hal.univ-brest.fr/hal-02042408
Contributor : Ghislaine Calvez Connect in order to contact the contributor
Submitted on : Wednesday, February 20, 2019 - 1:41:42 PM
Last modification on : Thursday, March 31, 2022 - 11:00:02 AM

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  • HAL Id : hal-02042408, version 1

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C. Hyon, L. Mansour-Hendili, S. Chantot-Bastaraud, B. Donadille, V. Kerlan, et al.. Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency. Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2016, 101 (5), pp.2099-2104. ⟨hal-02042408⟩

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