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authFullName_s : Marja Hietala
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A homozygous $FANCM$ mutation underlies a familial case of non-syndromic primary ovarian insufficiency

Baptiste Fouquet , Patrycja Pawlikowska , Sandrine Caburet , Céline Guigon , Marika Mäkinen et al.
eLife, 2017, 6, pp.e30490. ⟨10.7554/eLife.30490⟩
Journal articles hal-02391886v1
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Hypomorphic mutations of TRIP11 cause odontochondrodysplasia.

Anika Wehrle , Tomasz M Witkos , Sheila Unger , Judith Schneider , John A Follit et al.
JCI Insight, 2019, 4 (3), pp.e124701. ⟨10.1172/jci.insight.124701⟩
Journal articles hal-03664346v1