Associated Papers
Second family with the Boston-type craniosynostosis syndrome: novel mutation and expansion of the clinical spectrum.
Janssen A et al.
American Journal of Medical Genetics. Part A, 2013
A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly.
Ghassibé M et al.
European Journal of Pediatrics, 2006
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