Publications by authors named "V Milon"

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ARID2-related disorder: further delineation of the clinical phenotype of 27 novel individuals and description of an epigenetic signature.
Clara Houdayer, Kathleen Rooney, Liselot van der Laan, Céline Bris, Mariëlle Alders, Vincent Milon

Eur J Hum Genet· November 2025

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The recurrent p.Glu3Lys variant in is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalities.
P Rollier, A Cospain, M Barth, V Milon, N Gueguen

Mol Genet Metab Rep· June 2025

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Diagnosis of tuberous sclerosis in the prenatal period: a retrospective study of 240 cases and review of the literature.
Vincent Milon, Marie-Claire Malinge, Maud Blanluet, Marine Tessarech, Clarisse Battault

Eur J Hum Genet· December 2024

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Correction: Diagnosis of tuberous sclerosis in the prenatal period: a retrospective study of 240 cases and review of the literature.
Vincent Milon, Marie-Claire Malinge, Maud Blanluet, Marine Tessarech, Clarisse Battault

Eur J Hum Genet· July 2024

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Thrombotic microangiopathy with mild renal involvement and profound thrombocytopenia: not all roads lead to thrombotic thrombocytopenic purpura.
Victor Milon, Nicolas Fage, Fanny Guibert, Véronique Frémeaux-Bacchi, Jean-François Augusto

J Nephrol· May 2022

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