Delphine Minot - Ctr Genet, CHU Dijon

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Papers共 9 篇Author StatisticsCo-AuthorSimilar Experts

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A New Family with an SLC9A6 Mutation Expanding the Phenotypic Spectrum of Christianson Syndrome

Alice Masurel-Paulet,Amelie Piton,Sophie Chancenotte,Claire Redin,Christel Thauvin-Robinet, Yvan Henrenger,Delphine Minot, Audrey Creppy,Marie Ruffier-Bourdet,Julien Thevenon,Paul Kuentz,Daphne Lehalle,Aurore Curie,Gaelle Blanchard, Ezzat Ghosn,Marlene Bonnet, Melanie Archimbaud-Devilliers,Frederic Huet,Odile Perret,Nicole Philip,Jean-Louis Mandel,Laurence Faivre

American journal of medical genetics Part A（2016）

Cited16Views0WOSBibtex

Neuropsychological and neuroimaging phenotype induced by a CAMTA1 mutation

Eloi Magnin,Oleg Blagosklonov,Geraldine Sylvestre,Delphine Minot,Julien Thevenon,Laurence Faivre,Hatem Boulahdour,Christel Thauvin-Robinet,Lucien Rumbach

Brain & developmentno. 8 (2013): 711-5

Cited9Views0WOSBibtex

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