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 gene in a family with foramina parietalia permagna (FPP).
Spruijt L et al.
American Journal of Medical Genetics. Part A, 2005
Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.
Wuyts W et al.
Human Molecular Genetics, 2000
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