Search Results - Calis, Chantal M

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  1. 1
    Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause

    Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause by Theunissen, Tom E J, Nguyen, Minh, Kamps, Rick, Hendrickx, Alexandra T, Sallevelt, Suzanne C E H, Gottschalk, Ralph W H, Calis, Chantal M, Stassen, Alphons P M, de Koning, Bart, Mulder-Den Hartog, Elvira N M, Schoonderwoerd, Kees, Fuchs, Sabine A, Hilhorst-Hofstee, Yvonne, de Visser, Marianne, Vanoevelen, Jo, Szklarczyk, Radek, Gerards, Mike, de Coo, Irenaeus F M, Hellebrekers, Debby M E I, Smeets, Hubert J M

    Published in Frontiers in genetics
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  2. 2
    Identification of differential protein interactors of lamin A and progerin

    Identification of differential protein interactors of lamin A and progerin by Kubben, Nard, Voncken, Jan Willem, Demmers, Jeroen, Calis, Chantal, van Almen, Geert, Pinto, Yigal M., Misteli, Tom

    Published in Nucleus (Austin, Tex.)
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  3. 3
    Post-natal myogenic and adipogenic developmental: Defects and metabolic impairment upon loss of A-type lamins

    Post-natal myogenic and adipogenic developmental: Defects and metabolic impairment upon loss of A-type lamins by Kubben, Nard, Voncken, Jan Willem, Konings, Gonda, van Weeghel, Michel, van den Hoogenhof, Maarten M.G., Gijbels, Marion, van Erk, Arie, Schoonderwoerd, Kees, van den Bosch, Bianca, Dahlmans, Vivian, Calis, Chantal, Houten, Sander M., Misteli, Tom, Pinto, Yigal M.

    Published in Nucleus (Austin, Tex.)
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