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All Publications

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    • Journal article
    A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly.
    Ghassibé, Michella[UCL] Bernier, Vincent Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2006) European Journal of Pediatrics — Vol. 165, no. 10, p. 734-735 (2006)