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authFullName_s : Bettina Bessières
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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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Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy

Virginie Mariot , S. Roche , Débora Portilho , Sabrina Sacconi , Francesca Puppo et al.
Annals of Neurology, 2015, 78 (3), pp.387-400. ⟨10.1002/ana.24446⟩
Journal articles hal-01431338v1
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DUX4 and DUX4 downstream target genes are expressed in fetal FSHD muscles.

Maxime Ferreboeuf , Virginie Mariot , Bettina Bessières , Alexandre Vasiljevic , Tania Attié-Bitach et al.
Human Molecular Genetics, 2013, 23 (1), epub ahead of print. ⟨10.1093/hmg/ddt409⟩
Journal articles hal-00868855v1