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A homozygous $FANCM$ mutation underlies a familial case of non-syndromic primary ovarian insufficiencyeLife, 2017, 6, pp.e30490. ⟨10.7554/eLife.30490⟩
Journal articles
hal-02391886v1
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Hypomorphic mutations of TRIP11 cause odontochondrodysplasia.JCI Insight, 2019, 4 (3), pp.e124701. ⟨10.1172/jci.insight.124701⟩
Journal articles
hal-03664346v1
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