homozygous FANCM mutationn underlies a familial case of non-syndromic primary ovarian insufficiency - Archive ouverte HAL Access content directly
Journal Articles eLife Year : 2022

homozygous FANCM mutationn underlies a familial case of non-syndromic primary ovarian insufficiency

(1) ,
1
Roxanne Hablot
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hal-03886811 , version 1 (06-12-2022)

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  • HAL Id : hal-03886811 , version 1

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Rousselle Tr Théo, Roxanne Hablot. homozygous FANCM mutationn underlies a familial case of non-syndromic primary ovarian insufficiency. eLife, 2022. ⟨hal-03886811⟩
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