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	Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicism Stéphane Roche , Camille Dion , Natacha Broucqsault , Camille Laberthonnière , Marie-Cécile Gaillard Neurology Genetics, 2019, 5 (6), pp.e372. ⟨10.1212/NXG.0000000000000372⟩ Article dans une revue hal-02406985v1
	Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy Karine Nguyen , Francesca Puppo , Stéphane Roche , Marie-Cécile Gaillard , Charlene Chaix Human Mutation, 2017, 38 (10), pp.1432 - 1441. ⟨10.1002/humu.23304⟩ Article dans une revue hal-01614514v1

	3D nuclear topology dynamics of the 4q35 subtelomeric region linked to Facio-Scapulo-Humeral Dystrophy in skeletal muscle cells and hiPSC Camille Dion , Marie-Cécile Gaillard , Arnaud Lagarde , Cherif Badja , Armand Tasmadjian EMBO Conference - Chromatin and Epigenetics, May 2015, Heidelberg, Germany Poster de conférence hal-01675614v1

Frederique Magdinier