KBP–cytoskeleton interactions underlie developmental anomalies in Goldberg–Shprintzen syndrome.
Drévillon, Loïc; Megarbane, André; Demeer, Bénédicte; Matar, Corine; Benit, Paule; Briand-Suleau, Audrey; Bodereau, Virginie; Ghoumid, Jamal; Nasser, Mayssa; Decrouy, Xavier; Doco-Fenzy, Martine; Rustin, Pierre; Gaillard, Dominique; Goossens, Michel; Giurgea, Irina; Human Molecular Genetics, 2013, vol. 22, issue 12, p 2387, ISSN 09646906. ISBN 14602083.

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