Publications by authors named "C VoVan"

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Complex 4q35 and 10q26 Rearrangements: A Challenge for Molecular Diagnosis of Patients With Facioscapulohumeral Dystrophy.
Megane Delourme, Chaix Charlene, Laurene Gerard, Benjamin Ganne, Pierre Perrin, Catherine Vovan

Neurol Genet· June 2023

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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, Catherine Vovan

Neurol Genet· December 2019

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Deciphering the complexity of the 4q and 10q subtelomeres by molecular combing in healthy individuals and patients with facioscapulohumeral dystrophy.
Karine Nguyen, Natacha Broucqsault, Charlene Chaix, Stephane Roche, Jérôme D Robin, Catherine Vovan

J Med Genet· September 2019

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Inflammatory facioscapulohumeral muscular dystrophy type 2 in 18p deletion syndrome.
Dimitri Renard, Guillaume Taieb, Matteo Garibaldi, Andre Maues De Paula, Rafaelle Bernard, Catherine Vovan

Am J Med Genet A· August 2018

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[Comparison of citrate 4% and heparin as tunneled-catheters-locking solution in chronic hemodialysis].
Guillaume Chazot, Manolie Mehdi, Christie Lorriaux, Patrik Deleaval, Brice Mayor

Nephrol Ther· February 2018

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