Works matching AU Minot, Delphine

Results: 2
    1

    A new family with an SLC9A6 mutation expanding the phenotypic spectrum of Christianson syndrome.

    Published in:
    American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 8, p. 2103, doi. 10.1002/ajmg.a.37765
    By:
    • Masurel‐Paulet, Alice;
    • Piton, Amélie;
    • Chancenotte, Sophie;
    • Redin, Claire;
    • Thauvin‐Robinet, Christel;
    • Henrenger, Yvan;
    • Minot, Delphine;
    • Creppy, Audrey;
    • Ruffier‐Bourdet, Marie;
    • Thevenon, Julien;
    • Kuentz, Paul;
    • Lehalle, Daphné;
    • Curie, Aurore;
    • Blanchard, Gaelle;
    • Ghosn, Ezzat;
    • Bonnet, Marlene;
    • Archimbaud‐Devilliers, Mélanie;
    • Huet, Frédéric;
    • Perret, Odile;
    • Philip, Nicole
    Publication type:
    Article
    2

    12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 1, p. 82, doi. 10.1038/ejhg.2012.116
    By:
    • Thevenon, Julien;
    • Callier, Patrick;
    • Andrieux, Joris;
    • Delobel, Bruno;
    • David, Albert;
    • Sukno, Sylvie;
    • Minot, Delphine;
    • Mosca Anne, Laure;
    • Marle, Nathalie;
    • Sanlaville, Damien;
    • Bonnet, Marlène;
    • Masurel-Paulet, Alice;
    • Levy, Fabienne;
    • Gaunt, Lorraine;
    • Farrell, Sandra;
    • Le Caignec, Cédric;
    • Toutain, Annick;
    • Carmignac, Virginie;
    • Mugneret, Francine;
    • Clayton-Smith, Jill
    Publication type:
    Article