A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly.
(2006) European Journal of Pediatrics — Vol. 165, n° 10, p. 734-735 (2006)
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Ghassibé, M., Bernier, V., Boon, L., & Vikkula, M. (2006). A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly. European Journal of Pediatrics, 165(10), 734-735. https://doi.org/10.1007/s00431-006-0138-8 (Original work published 2006)